Canonical Allele Identifier: CA343773582

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878746T>C (hg19) ; chr1:g.173909608T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909608T>C , CM000663.2:g.173909608T>C	GRCh38
NC_000001.10:g.173878746T>C , CM000663.1:g.173878746T>C	GRCh37
NC_000001.9:g.172145369T>C	NCBI36
NG_012462.1:g.12771A>G , LRG_577:g.12771A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1097A>G MANE Select	ENSP00000356671.3:p.Gln366Arg
ENST00000367698.3:c.1097A>G	ENSP00000356671.3:p.Gln366Arg
ENST00000617423.4:c.560-2115A>G	ENSP00000478688.1:n.560-2115A>G
NM_000488.3:c.1097A>G , LRG_577t1:c.1097A>G	NP_000479.1:p.Gln366Arg
XM_005245198.2:c.953A>G	XP_005245255.1:p.Gln318Arg
NM_001365052.1:c.953A>G	NP_001351981.1:p.Gln318Arg
NM_000488.4:c.1097A>G MANE Select	NP_000479.1:p.Gln366Arg
NM_001365052.2:c.953A>G	NP_001351981.1:p.Gln318Arg
NM_001386302.1:c.1220A>G	NP_001373231.1:p.Gln407Arg
NM_001386303.1:c.1178A>G	NP_001373232.1:p.Gln393Arg
NM_001386304.1:c.1076A>G	NP_001373233.1:p.Gln359Arg
NM_001386305.1:c.1040A>G	NP_001373234.1:p.Gln347Arg
NM_001386306.1:c.881A>G	NP_001373235.1:p.Gln294Arg