Canonical Allele Identifier: CA343773914
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs1317476052

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909703C>A , CM000663.2:g.173909703C>A GRCh38
NC_000001.10:g.173878841C>A , CM000663.1:g.173878841C>A GRCh37
NC_000001.9:g.172145464C>A NCBI36
NG_012462.1:g.12676G>T , LRG_577:g.12676G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1002G>T MANE Select ENSP00000356671.3:p.Glu334Asp
ENST00000367698.3:c.1002G>T ENSP00000356671.3:p.Glu334Asp
ENST00000617423.4:c.559+2161G>T ENSP00000478688.1:n.559+2161G>T
NM_000488.3:c.1002G>T , LRG_577t1:c.1002G>T NP_000479.1:p.Glu334Asp
XM_005245198.2:c.858G>T XP_005245255.1:p.Glu286Asp
NM_001365052.1:c.858G>T NP_001351981.1:p.Glu286Asp
NM_000488.4:c.1002G>T MANE Select NP_000479.1:p.Glu334Asp
NM_001365052.2:c.858G>T NP_001351981.1:p.Glu286Asp
NM_001386302.1:c.1125G>T NP_001373231.1:p.Glu375Asp
NM_001386303.1:c.1083G>T NP_001373232.1:p.Glu361Asp
NM_001386304.1:c.981G>T NP_001373233.1:p.Glu327Asp
NM_001386305.1:c.945G>T NP_001373234.1:p.Glu315Asp
NM_001386306.1:c.786G>T NP_001373235.1:p.Glu262Asp