Canonical Allele Identifier: CA343773920

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878842T>C (hg19) ; chr1:g.173909704T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909704T>C , CM000663.2:g.173909704T>C	GRCh38
NC_000001.10:g.173878842T>C , CM000663.1:g.173878842T>C	GRCh37
NC_000001.9:g.172145465T>C	NCBI36
NG_012462.1:g.12675A>G , LRG_577:g.12675A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1001A>G MANE Select	ENSP00000356671.3:p.Glu334Gly
ENST00000367698.3:c.1001A>G	ENSP00000356671.3:p.Glu334Gly
ENST00000617423.4:c.559+2160A>G	ENSP00000478688.1:n.559+2160A>G
NM_000488.3:c.1001A>G , LRG_577t1:c.1001A>G	NP_000479.1:p.Glu334Gly
XM_005245198.2:c.857A>G	XP_005245255.1:p.Glu286Gly
NM_001365052.1:c.857A>G	NP_001351981.1:p.Glu286Gly
NM_000488.4:c.1001A>G MANE Select	NP_000479.1:p.Glu334Gly
NM_001365052.2:c.857A>G	NP_001351981.1:p.Glu286Gly
NM_001386302.1:c.1124A>G	NP_001373231.1:p.Glu375Gly
NM_001386303.1:c.1082A>G	NP_001373232.1:p.Glu361Gly
NM_001386304.1:c.980A>G	NP_001373233.1:p.Glu327Gly
NM_001386305.1:c.944A>G	NP_001373234.1:p.Glu315Gly
NM_001386306.1:c.785A>G	NP_001373235.1:p.Glu262Gly