Canonical Allele Identifier: CA210752
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18009
ClinVar RCV Id: RCV000019625
dbSNP Id: rs121909549

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904010C>G , CM000663.2:g.173904010C>G GRCh38
NC_000001.10:g.173873148C>G , CM000663.1:g.173873148C>G GRCh37
NC_000001.9:g.172139771C>G NCBI36
NG_012462.1:g.18369G>C , LRG_577:g.18369G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1274G>C MANE Select ENSP00000356671.3:p.Arg425Pro
ENST00000367698.3:c.1274G>C ENSP00000356671.3:p.Arg425Pro
ENST00000617423.4:c.659G>C ENSP00000478688.1:p.Arg220Pro
NM_000488.3:c.1274G>C , LRG_577t1:c.1274G>C NP_000479.1:p.Arg425Pro
XM_005245198.2:c.1130G>C XP_005245255.1:p.Arg377Pro
NM_001365052.1:c.1130G>C NP_001351981.1:p.Arg377Pro
NM_000488.4:c.1274G>C MANE Select NP_000479.1:p.Arg425Pro
NM_001365052.2:c.1130G>C NP_001351981.1:p.Arg377Pro
NM_001386302.1:c.1397G>C NP_001373231.1:p.Arg466Pro
NM_001386303.1:c.1355G>C NP_001373232.1:p.Arg452Pro
NM_001386304.1:c.1253G>C NP_001373233.1:p.Arg418Pro
NM_001386305.1:c.1217G>C NP_001373234.1:p.Arg406Pro
NM_001386306.1:c.1058G>C NP_001373235.1:p.Arg353Pro