Canonical Allele Identifier: CA343774316
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878939G>A (hg19) chr1:g.173909801G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909801G>A , CM000663.2:g.173909801G>A GRCh38
NC_000001.10:g.173878939G>A , CM000663.1:g.173878939G>A GRCh37
NC_000001.9:g.172145562G>A NCBI36
NG_012462.1:g.12578C>T , LRG_577:g.12578C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.904C>T MANE Select ENSP00000356671.3:p.Leu302Phe
ENST00000367698.3:c.904C>T ENSP00000356671.3:p.Leu302Phe
ENST00000487183.1:n.555C>T
ENST00000617423.4:c.559+2063C>T ENSP00000478688.1:n.559+2063C>T
NM_000488.3:c.904C>T , LRG_577t1:c.904C>T NP_000479.1:p.Leu302Phe
XM_005245198.2:c.760C>T XP_005245255.1:p.Leu254Phe
NM_001365052.1:c.760C>T NP_001351981.1:p.Leu254Phe
NM_000488.4:c.904C>T MANE Select NP_000479.1:p.Leu302Phe
NM_001365052.2:c.760C>T NP_001351981.1:p.Leu254Phe
NM_001386302.1:c.1027C>T NP_001373231.1:p.Leu343Phe
NM_001386303.1:c.985C>T NP_001373232.1:p.Leu329Phe
NM_001386304.1:c.883C>T NP_001373233.1:p.Leu295Phe
NM_001386305.1:c.847C>T NP_001373234.1:p.Leu283Phe
NM_001386306.1:c.688C>T NP_001373235.1:p.Leu230Phe
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