Canonical Allele Identifier: CA343774348
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909809G>A , CM000663.2:g.173909809G>A GRCh38
NC_000001.10:g.173878947G>A , CM000663.1:g.173878947G>A GRCh37
NC_000001.9:g.172145570G>A NCBI36
NG_012462.1:g.12570C>T , LRG_577:g.12570C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.896C>T MANE Select ENSP00000356671.3:p.Thr299Ile
ENST00000367698.3:c.896C>T ENSP00000356671.3:p.Thr299Ile
ENST00000487183.1:n.547C>T
ENST00000617423.4:c.559+2055C>T ENSP00000478688.1:n.559+2055C>T
NM_000488.3:c.896C>T , LRG_577t1:c.896C>T NP_000479.1:p.Thr299Ile
XM_005245198.2:c.752C>T XP_005245255.1:p.Thr251Ile
NM_001365052.1:c.752C>T NP_001351981.1:p.Thr251Ile
NM_000488.4:c.896C>T MANE Select NP_000479.1:p.Thr299Ile
NM_001365052.2:c.752C>T NP_001351981.1:p.Thr251Ile
NM_001386302.1:c.1019C>T NP_001373231.1:p.Thr340Ile
NM_001386303.1:c.977C>T NP_001373232.1:p.Thr326Ile
NM_001386304.1:c.875C>T NP_001373233.1:p.Thr292Ile
NM_001386305.1:c.839C>T NP_001373234.1:p.Thr280Ile
NM_001386306.1:c.680C>T NP_001373235.1:p.Thr227Ile