Canonical Allele Identifier: CA343774732
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879040T>A (hg19) chr1:g.173909902T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909902T>A , CM000663.2:g.173909902T>A GRCh38
NC_000001.10:g.173879040T>A , CM000663.1:g.173879040T>A GRCh37
NC_000001.9:g.172145663T>A NCBI36
NG_012462.1:g.12477A>T , LRG_577:g.12477A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.803A>T MANE Select ENSP00000356671.3:p.Lys268Met
ENST00000367698.3:c.803A>T ENSP00000356671.3:p.Lys268Met
ENST00000487183.1:n.454A>T
ENST00000617423.4:c.559+1962A>T ENSP00000478688.1:n.559+1962A>T
NM_000488.3:c.803A>T , LRG_577t1:c.803A>T NP_000479.1:p.Lys268Met
XM_005245198.2:c.659A>T XP_005245255.1:p.Lys220Met
NM_001365052.1:c.659A>T NP_001351981.1:p.Lys220Met
NM_000488.4:c.803A>T MANE Select NP_000479.1:p.Lys268Met
NM_001365052.2:c.659A>T NP_001351981.1:p.Lys220Met
NM_001386302.1:c.926A>T NP_001373231.1:p.Lys309Met
NM_001386303.1:c.884A>T NP_001373232.1:p.Lys295Met
NM_001386304.1:c.782A>T NP_001373233.1:p.Lys261Met
NM_001386305.1:c.763-17A>T NP_001373234.1:n.763-17A>T
NM_001386306.1:c.587A>T NP_001373235.1:p.Lys196Met
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