Canonical Allele Identifier: CA1207934370
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173903946T= , CM000663.2:g.173903946T= GRCh38
NC_000001.10:g.173873084T= , CM000663.1:g.173873084T= GRCh37
NC_000001.9:g.172139707T= NCBI36
NG_012462.1:g.18433A= , LRG_577:g.18433A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1338A= MANE Select ENSP00000356671.3:p.Glu446=
ENST00000367698.3:c.1338A= ENSP00000356671.3:p.Glu446=
ENST00000617423.4:c.723A= ENSP00000478688.1:p.Glu241=
NM_000488.3:c.1338A= , LRG_577t1:c.1338A= NP_000479.1:p.Glu446=
XM_005245198.2:c.1194A= XP_005245255.1:p.Glu398=
NM_001365052.1:c.1194A= NP_001351981.1:p.Glu398=
NM_000488.4:c.1338A= MANE Select NP_000479.1:p.Glu446=
NM_001365052.2:c.1194A= NP_001351981.1:p.Glu398=
NM_001386302.1:c.1461A= NP_001373231.1:p.Glu487=
NM_001386303.1:c.1419A= NP_001373232.1:p.Glu473=
NM_001386304.1:c.1317A= NP_001373233.1:p.Glu439=
NM_001386305.1:c.1281A= NP_001373234.1:p.Glu427=
NM_001386306.1:c.1122A= NP_001373235.1:p.Glu374=