Canonical Allele Identifier: CA343772643
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173873178G>A (hg19) chr1:g.173904040G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904040G>A , CM000663.2:g.173904040G>A GRCh38
NC_000001.10:g.173873178G>A , CM000663.1:g.173873178G>A GRCh37
NC_000001.9:g.172139801G>A NCBI36
NG_012462.1:g.18339C>T , LRG_577:g.18339C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1244C>T MANE Select ENSP00000356671.3:p.Ala415Val
ENST00000367698.3:c.1244C>T ENSP00000356671.3:p.Ala415Val
ENST00000617423.4:c.629C>T ENSP00000478688.1:p.Ala210Val
NM_000488.3:c.1244C>T , LRG_577t1:c.1244C>T NP_000479.1:p.Ala415Val
XM_005245198.2:c.1100C>T XP_005245255.1:p.Ala367Val
NM_001365052.1:c.1100C>T NP_001351981.1:p.Ala367Val
NM_000488.4:c.1244C>T MANE Select NP_000479.1:p.Ala415Val
NM_001365052.2:c.1100C>T NP_001351981.1:p.Ala367Val
NM_001386302.1:c.1367C>T NP_001373231.1:p.Ala456Val
NM_001386303.1:c.1325C>T NP_001373232.1:p.Ala442Val
NM_001386304.1:c.1223C>T NP_001373233.1:p.Ala408Val
NM_001386305.1:c.1187C>T NP_001373234.1:p.Ala396Val
NM_001386306.1:c.1028C>T NP_001373235.1:p.Ala343Val
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