Canonical Allele Identifier: CA343774749
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909909T>G , CM000663.2:g.173909909T>G GRCh38
NC_000001.10:g.173879047T>G , CM000663.1:g.173879047T>G GRCh37
NC_000001.9:g.172145670T>G NCBI36
NG_012462.1:g.12470A>C , LRG_577:g.12470A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.796A>C MANE Select ENSP00000356671.3:p.Thr266Pro
ENST00000367698.3:c.796A>C ENSP00000356671.3:p.Thr266Pro
ENST00000487183.1:n.447A>C
ENST00000617423.4:c.559+1955A>C ENSP00000478688.1:n.559+1955A>C
NM_000488.3:c.796A>C , LRG_577t1:c.796A>C NP_000479.1:p.Thr266Pro
XM_005245198.2:c.652A>C XP_005245255.1:p.Thr218Pro
NM_001365052.1:c.652A>C NP_001351981.1:p.Thr218Pro
NM_000488.4:c.796A>C MANE Select NP_000479.1:p.Thr266Pro
NM_001365052.2:c.652A>C NP_001351981.1:p.Thr218Pro
NM_001386302.1:c.919A>C NP_001373231.1:p.Thr307Pro
NM_001386303.1:c.877A>C NP_001373232.1:p.Thr293Pro
NM_001386304.1:c.775A>C NP_001373233.1:p.Thr259Pro
NM_001386305.1:c.763-24A>C NP_001373234.1:n.763-24A>C
NM_001386306.1:c.580A>C NP_001373235.1:p.Thr194Pro