Canonical Allele Identifier: CA343778352
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173914848T>A , CM000663.2:g.173914848T>A GRCh38
NC_000001.10:g.173883986T>A , CM000663.1:g.173883986T>A GRCh37
NC_000001.9:g.172150609T>A NCBI36
NG_012462.1:g.7531A>T , LRG_577:g.7531A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.113A>T MANE Select ENSP00000356671.3:p.Asp38Val
ENST00000367698.3:c.113A>T ENSP00000356671.3:p.Asp38Val
ENST00000494024.1:n.339A>T
ENST00000617423.4:c.113A>T ENSP00000478688.1:p.Asp38Val
NM_000488.3:c.113A>T , LRG_577t1:c.113A>T NP_000479.1:p.Asp38Val
XM_005245198.2:c.-32A>T XP_005245255.1:n.-32A>T
NM_001365052.1:c.-32A>T NP_001351981.1:n.-32A>T
NM_000488.4:c.113A>T MANE Select NP_000479.1:p.Asp38Val
NM_001365052.2:c.-32A>T NP_001351981.1:n.-32A>T
NM_001386302.1:c.113A>T NP_001373231.1:p.Asp38Val
NM_001386303.1:c.194A>T NP_001373232.1:p.Asp65Val
NM_001386304.1:c.113A>T NP_001373233.1:p.Asp38Val
NM_001386305.1:c.113A>T NP_001373234.1:p.Asp38Val
NM_001386306.1:c.113A>T NP_001373235.1:p.Asp38Val