Canonical Allele Identifier: CA343772556
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904002T>A , CM000663.2:g.173904002T>A GRCh38
NC_000001.10:g.173873140T>A , CM000663.1:g.173873140T>A GRCh37
NC_000001.9:g.172139763T>A NCBI36
NG_012462.1:g.18377A>T , LRG_577:g.18377A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1282A>T MANE Select ENSP00000356671.3:p.Asn428Tyr
ENST00000367698.3:c.1282A>T ENSP00000356671.3:p.Asn428Tyr
ENST00000617423.4:c.667A>T ENSP00000478688.1:p.Asn223Tyr
NM_000488.3:c.1282A>T , LRG_577t1:c.1282A>T NP_000479.1:p.Asn428Tyr
XM_005245198.2:c.1138A>T XP_005245255.1:p.Asn380Tyr
NM_001365052.1:c.1138A>T NP_001351981.1:p.Asn380Tyr
NM_000488.4:c.1282A>T MANE Select NP_000479.1:p.Asn428Tyr
NM_001365052.2:c.1138A>T NP_001351981.1:p.Asn380Tyr
NM_001386302.1:c.1405A>T NP_001373231.1:p.Asn469Tyr
NM_001386303.1:c.1363A>T NP_001373232.1:p.Asn455Tyr
NM_001386304.1:c.1261A>T NP_001373233.1:p.Asn421Tyr
NM_001386305.1:c.1225A>T NP_001373234.1:p.Asn409Tyr
NM_001386306.1:c.1066A>T NP_001373235.1:p.Asn356Tyr