Canonical Allele Identifier: CA1207936880
Gene: SERPINC1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909515_173909519delinsCGGGT , CM000663.2:g.173909515_173909519delinsCGGGT GRCh38
NC_000001.10:g.173878653_173878657delinsCGGGT , CM000663.1:g.173878653_173878657delinsCGGGT GRCh37
NC_000001.9:g.172145276_172145280delinsCGGGT NCBI36
NG_012462.1:g.12860_12864delinsACCCG , LRG_577:g.12860_12864delinsACCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1153+33_1153+37delinsACCCG MANE Select ENSP00000356671.3:n.1153+33_1153+37delinsACCCG
ENST00000367698.3:c.1153+33_1153+37delinsACCCG ENSP00000356671.3:n.1153+33_1153+37delinsACCCG
ENST00000617423.4:c.560-2026_560-2022delinsACCCG ENSP00000478688.1:n.560-2026_560-2022delinsACCCG
NM_000488.3:c.1153+33_1153+37delinsACCCG , LRG_577t1:c.1153+33_1153+37delinsACCCG NP_000479.1:n.1153+33_1153+37delinsACCCG
XM_005245198.2:c.1009+33_1009+37delinsACCCG XP_005245255.1:n.1009+33_1009+37delinsACCCG
NM_001365052.1:c.1009+33_1009+37delinsACCCG NP_001351981.1:n.1009+33_1009+37delinsACCCG
NM_000488.4:c.1153+33_1153+37delinsACCCG MANE Select NP_000479.1:n.1153+33_1153+37delinsACCCG
NM_001365052.2:c.1009+33_1009+37delinsACCCG NP_001351981.1:n.1009+33_1009+37delinsACCCG
NM_001386302.1:c.1276+33_1276+37delinsACCCG NP_001373231.1:n.1276+33_1276+37delinsACCCG
NM_001386303.1:c.1234+33_1234+37delinsACCCG NP_001373232.1:n.1234+33_1234+37delinsACCCG
NM_001386304.1:c.1132+33_1132+37delinsACCCG NP_001373233.1:n.1132+33_1132+37delinsACCCG
NM_001386305.1:c.1096+33_1096+37delinsACCCG NP_001373234.1:n.1096+33_1096+37delinsACCCG
NM_001386306.1:c.937+33_937+37delinsACCCG NP_001373235.1:n.937+33_937+37delinsACCCG
Search 100 bp 5'
Search 100 bp 3'