Canonical Allele Identifier: CA343773874

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878831C>G (hg19) ; chr1:g.173909693C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909693C>G , CM000663.2:g.173909693C>G	GRCh38
NC_000001.10:g.173878831C>G , CM000663.1:g.173878831C>G	GRCh37
NC_000001.9:g.172145454C>G	NCBI36
NG_012462.1:g.12686G>C , LRG_577:g.12686G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1012G>C MANE Select	ENSP00000356671.3:p.Glu338Gln
ENST00000367698.3:c.1012G>C	ENSP00000356671.3:p.Glu338Gln
ENST00000617423.4:c.559+2171G>C	ENSP00000478688.1:n.559+2171G>C
NM_000488.3:c.1012G>C , LRG_577t1:c.1012G>C	NP_000479.1:p.Glu338Gln
XM_005245198.2:c.868G>C	XP_005245255.1:p.Glu290Gln
NM_001365052.1:c.868G>C	NP_001351981.1:p.Glu290Gln
NM_000488.4:c.1012G>C MANE Select	NP_000479.1:p.Glu338Gln
NM_001365052.2:c.868G>C	NP_001351981.1:p.Glu290Gln
NM_001386302.1:c.1135G>C	NP_001373231.1:p.Glu379Gln
NM_001386303.1:c.1093G>C	NP_001373232.1:p.Glu365Gln
NM_001386304.1:c.991G>C	NP_001373233.1:p.Glu331Gln
NM_001386305.1:c.955G>C	NP_001373234.1:p.Glu319Gln
NM_001386306.1:c.796G>C	NP_001373235.1:p.Glu266Gln