Canonical Allele Identifier: CA1207936922
Gene: SERPINC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909634A= , CM000663.2:g.173909634A= GRCh38
NC_000001.10:g.173878772A= , CM000663.1:g.173878772A= GRCh37
NC_000001.9:g.172145395A= NCBI36
NG_012462.1:g.12745T= , LRG_577:g.12745T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1071T= MANE Select ENSP00000356671.3:p.Ile357=
ENST00000367698.3:c.1071T= ENSP00000356671.3:p.Ile357=
ENST00000617423.4:c.560-2141T= ENSP00000478688.1:n.560-2141T=
NM_000488.3:c.1071T= , LRG_577t1:c.1071T= NP_000479.1:p.Ile357=
XM_005245198.2:c.927T= XP_005245255.1:p.Ile309=
NM_001365052.1:c.927T= NP_001351981.1:p.Ile309=
NM_000488.4:c.1071T= MANE Select NP_000479.1:p.Ile357=
NM_001365052.2:c.927T= NP_001351981.1:p.Ile309=
NM_001386302.1:c.1194T= NP_001373231.1:p.Ile398=
NM_001386303.1:c.1152T= NP_001373232.1:p.Ile384=
NM_001386304.1:c.1050T= NP_001373233.1:p.Ile350=
NM_001386305.1:c.1014T= NP_001373234.1:p.Ile338=
NM_001386306.1:c.855T= NP_001373235.1:p.Ile285=