Canonical Allele Identifier: CA1207936316
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173908275A= , CM000663.2:g.173908275A= GRCh38
NC_000001.10:g.173877413A= , CM000663.1:g.173877413A= GRCh37
NC_000001.9:g.172144036A= NCBI36
NG_012462.1:g.14104T= , LRG_577:g.14104T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.1154-761T= MANE Select ENSP00000356671.3:n.1154-761T=
ENST00000367698.3:c.1154-761T= ENSP00000356671.3:n.1154-761T=
ENST00000617423.4:c.560-782T= ENSP00000478688.1:n.560-782T=
NM_000488.3:c.1154-761T= , LRG_577t1:c.1154-761T= NP_000479.1:n.1154-761T=
XM_005245198.2:c.1010-761T= XP_005245255.1:n.1010-761T=
NM_001365052.1:c.1010-761T= NP_001351981.1:n.1010-761T=
NM_000488.4:c.1154-761T= MANE Select NP_000479.1:n.1154-761T=
NM_001365052.2:c.1010-761T= NP_001351981.1:n.1010-761T=
NM_001386302.1:c.1277-761T= NP_001373231.1:n.1277-761T=
NM_001386303.1:c.1235-761T= NP_001373232.1:n.1235-761T=
NM_001386304.1:c.1133-761T= NP_001373233.1:n.1133-761T=
NM_001386305.1:c.1097-761T= NP_001373234.1:n.1097-761T=
NM_001386306.1:c.938-761T= NP_001373235.1:n.938-761T=