Canonical Allele Identifier: CA343774377

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1572088644
• gnomAD v4: 1-173909815-T-G
• MyVariant Identifiers: chr1:g.173878953T>G (hg19) ; chr1:g.173909815T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909815T>G , CM000663.2:g.173909815T>G	GRCh38
NC_000001.10:g.173878953T>G , CM000663.1:g.173878953T>G	GRCh37
NC_000001.9:g.172145576T>G	NCBI36
NG_012462.1:g.12564A>C , LRG_577:g.12564A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.890A>C MANE Select	ENSP00000356671.3:p.Glu297Ala
ENST00000367698.3:c.890A>C	ENSP00000356671.3:p.Glu297Ala
ENST00000487183.1:n.541A>C
ENST00000617423.4:c.559+2049A>C	ENSP00000478688.1:n.559+2049A>C
NM_000488.3:c.890A>C , LRG_577t1:c.890A>C	NP_000479.1:p.Glu297Ala
XM_005245198.2:c.746A>C	XP_005245255.1:p.Glu249Ala
NM_001365052.1:c.746A>C	NP_001351981.1:p.Glu249Ala
NM_000488.4:c.890A>C MANE Select	NP_000479.1:p.Glu297Ala
NM_001365052.2:c.746A>C	NP_001351981.1:p.Glu249Ala
NM_001386302.1:c.1013A>C	NP_001373231.1:p.Glu338Ala
NM_001386303.1:c.971A>C	NP_001373232.1:p.Glu324Ala
NM_001386304.1:c.869A>C	NP_001373233.1:p.Glu290Ala
NM_001386305.1:c.833A>C	NP_001373234.1:p.Glu278Ala
NM_001386306.1:c.674A>C	NP_001373235.1:p.Glu225Ala