Canonical Allele Identifier: CA343774608
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909870A>T , CM000663.2:g.173909870A>T GRCh38
NC_000001.10:g.173879008A>T , CM000663.1:g.173879008A>T GRCh37
NC_000001.9:g.172145631A>T NCBI36
NG_012462.1:g.12509T>A , LRG_577:g.12509T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.835T>A MANE Select ENSP00000356671.3:p.Cys279Ser
ENST00000367698.3:c.835T>A ENSP00000356671.3:p.Cys279Ser
ENST00000487183.1:n.486T>A
ENST00000617423.4:c.559+1994T>A ENSP00000478688.1:n.559+1994T>A
NM_000488.3:c.835T>A , LRG_577t1:c.835T>A NP_000479.1:p.Cys279Ser
XM_005245198.2:c.691T>A XP_005245255.1:p.Cys231Ser
NM_001365052.1:c.691T>A NP_001351981.1:p.Cys231Ser
NM_000488.4:c.835T>A MANE Select NP_000479.1:p.Cys279Ser
NM_001365052.2:c.691T>A NP_001351981.1:p.Cys231Ser
NM_001386302.1:c.958T>A NP_001373231.1:p.Cys320Ser
NM_001386303.1:c.916T>A NP_001373232.1:p.Cys306Ser
NM_001386304.1:c.814T>A NP_001373233.1:p.Cys272Ser
NM_001386305.1:c.778T>A NP_001373234.1:p.Cys260Ser
NM_001386306.1:c.619T>A NP_001373235.1:p.Cys207Ser