Canonical Allele Identifier: CA1207934382
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903997G= , CM000663.2:g.173903997G= GRCh38
NC_000001.10:g.173873135G= , CM000663.1:g.173873135G= GRCh37
NC_000001.9:g.172139758G= NCBI36
NG_012462.1:g.18382C= , LRG_577:g.18382C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1287C= MANE Select ENSP00000356671.3:p.Pro429=
ENST00000367698.3:c.1287C= ENSP00000356671.3:p.Pro429=
ENST00000617423.4:c.672C= ENSP00000478688.1:p.Pro224=
NM_000488.3:c.1287C= , LRG_577t1:c.1287C= NP_000479.1:p.Pro429=
XM_005245198.2:c.1143C= XP_005245255.1:p.Pro381=
NM_001365052.1:c.1143C= NP_001351981.1:p.Pro381=
NM_000488.4:c.1287C= MANE Select NP_000479.1:p.Pro429=
NM_001365052.2:c.1143C= NP_001351981.1:p.Pro381=
NM_001386302.1:c.1410C= NP_001373231.1:p.Pro470=
NM_001386303.1:c.1368C= NP_001373232.1:p.Pro456=
NM_001386304.1:c.1266C= NP_001373233.1:p.Pro422=
NM_001386305.1:c.1230C= NP_001373234.1:p.Pro410=
NM_001386306.1:c.1071C= NP_001373235.1:p.Pro357=