Canonical Allele Identifier: CA343774065

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173909740-T-C
• MyVariant Identifiers: chr1:g.173878878T>C (hg19) ; chr1:g.173909740T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909740T>C , CM000663.2:g.173909740T>C	GRCh38
NC_000001.10:g.173878878T>C , CM000663.1:g.173878878T>C	GRCh37
NC_000001.9:g.172145501T>C	NCBI36
NG_012462.1:g.12639A>G , LRG_577:g.12639A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.965A>G MANE Select	ENSP00000356671.3:p.Lys322Arg
ENST00000367698.3:c.965A>G	ENSP00000356671.3:p.Lys322Arg
ENST00000487183.1:n.616A>G
ENST00000617423.4:c.559+2124A>G	ENSP00000478688.1:n.559+2124A>G
NM_000488.3:c.965A>G , LRG_577t1:c.965A>G	NP_000479.1:p.Lys322Arg
XM_005245198.2:c.821A>G	XP_005245255.1:p.Lys274Arg
NM_001365052.1:c.821A>G	NP_001351981.1:p.Lys274Arg
NM_000488.4:c.965A>G MANE Select	NP_000479.1:p.Lys322Arg
NM_001365052.2:c.821A>G	NP_001351981.1:p.Lys274Arg
NM_001386302.1:c.1088A>G	NP_001373231.1:p.Lys363Arg
NM_001386303.1:c.1046A>G	NP_001373232.1:p.Lys349Arg
NM_001386304.1:c.944A>G	NP_001373233.1:p.Lys315Arg
NM_001386305.1:c.908A>G	NP_001373234.1:p.Lys303Arg
NM_001386306.1:c.749A>G	NP_001373235.1:p.Lys250Arg