Canonical Allele Identifier: CA421942798
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879044T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909906T>G , CM000663.2:g.173909906T>G GRCh38
NC_000001.10:g.173879044T>G , CM000663.1:g.173879044T>G GRCh37
NC_000001.9:g.172145667T>G NCBI36
NG_012462.1:g.12473A>C , LRG_577:g.12473A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.799A>C MANE Select ENSP00000356671.3:p.Arg267=
ENST00000367698.3:c.799A>C ENSP00000356671.3:p.Arg267=
ENST00000487183.1:n.450A>C
ENST00000617423.4:c.559+1958A>C ENSP00000478688.1:n.559+1958A>C
NM_000488.3:c.799A>C , LRG_577t1:c.799A>C NP_000479.1:p.Arg267=
XM_005245198.2:c.655A>C XP_005245255.1:p.Arg219=
NM_001365052.1:c.655A>C NP_001351981.1:p.Arg219=
NM_000488.4:c.799A>C MANE Select NP_000479.1:p.Arg267=
NM_001365052.2:c.655A>C NP_001351981.1:p.Arg219=
NM_001386302.1:c.922A>C NP_001373231.1:p.Arg308=
NM_001386303.1:c.880A>C NP_001373232.1:p.Arg294=
NM_001386304.1:c.778A>C NP_001373233.1:p.Arg260=
NM_001386305.1:c.763-21A>C NP_001373234.1:n.763-21A>C
NM_001386306.1:c.583A>C NP_001373235.1:p.Arg195=
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