Canonical Allele Identifier: CA343774806
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879070T>G (hg19) chr1:g.173909932T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909932T>G , CM000663.2:g.173909932T>G GRCh38
NC_000001.10:g.173879070T>G , CM000663.1:g.173879070T>G GRCh37
NC_000001.9:g.172145693T>G NCBI36
NG_012462.1:g.12447A>C , LRG_577:g.12447A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.773A>C MANE Select ENSP00000356671.3:p.Lys258Thr
ENST00000367698.3:c.773A>C ENSP00000356671.3:p.Lys258Thr
ENST00000487183.1:n.424A>C
ENST00000617423.4:c.559+1932A>C ENSP00000478688.1:n.559+1932A>C
NM_000488.3:c.773A>C , LRG_577t1:c.773A>C NP_000479.1:p.Lys258Thr
XM_005245198.2:c.629A>C XP_005245255.1:p.Lys210Thr
NM_001365052.1:c.629A>C NP_001351981.1:p.Lys210Thr
NM_000488.4:c.773A>C MANE Select NP_000479.1:p.Lys258Thr
NM_001365052.2:c.629A>C NP_001351981.1:p.Lys210Thr
NM_001386302.1:c.896A>C NP_001373231.1:p.Lys299Thr
NM_001386303.1:c.854A>C NP_001373232.1:p.Lys285Thr
NM_001386304.1:c.752A>C NP_001373233.1:p.Lys251Thr
NM_001386305.1:c.763-47A>C NP_001373234.1:n.763-47A>C
NM_001386306.1:c.557A>C NP_001373235.1:p.Lys186Thr
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