Canonical Allele Identifier: CA2697768540
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs2102773542

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904156dup , CM000663.2:g.173904156dup GRCh38
NC_000001.10:g.173873294dup , CM000663.1:g.173873294dup GRCh37
NC_000001.9:g.172139917dup NCBI36
NG_012462.1:g.18225dup , LRG_577:g.18225dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1219-89dup MANE Select ENSP00000356671.3:n.1219-89dup
ENST00000367698.3:c.1219-89dup ENSP00000356671.3:n.1219-89dup
ENST00000617423.4:c.604-89dup ENSP00000478688.1:n.604-89dup
NM_000488.3:c.1219-89dup , LRG_577t1:c.1219-89dup NP_000479.1:n.1219-89dup
XM_005245198.2:c.1075-89dup XP_005245255.1:n.1075-89dup
NM_001365052.1:c.1075-89dup NP_001351981.1:n.1075-89dup
NM_000488.4:c.1219-89dup MANE Select NP_000479.1:n.1219-89dup
NM_001365052.2:c.1075-89dup NP_001351981.1:n.1075-89dup
NM_001386302.1:c.1342-89dup NP_001373231.1:n.1342-89dup
NM_001386303.1:c.1300-89dup NP_001373232.1:n.1300-89dup
NM_001386304.1:c.1198-89dup NP_001373233.1:n.1198-89dup
NM_001386305.1:c.1162-89dup NP_001373234.1:n.1162-89dup
NM_001386306.1:c.1003-89dup NP_001373235.1:n.1003-89dup