Canonical Allele Identifier: CA343773949

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878849T>C (hg19) ; chr1:g.173909711T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909711T>C , CM000663.2:g.173909711T>C	GRCh38
NC_000001.10:g.173878849T>C , CM000663.1:g.173878849T>C	GRCh37
NC_000001.9:g.172145472T>C	NCBI36
NG_012462.1:g.12668A>G , LRG_577:g.12668A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.994A>G MANE Select	ENSP00000356671.3:p.Thr332Ala
ENST00000367698.3:c.994A>G	ENSP00000356671.3:p.Thr332Ala
ENST00000617423.4:c.559+2153A>G	ENSP00000478688.1:n.559+2153A>G
NM_000488.3:c.994A>G , LRG_577t1:c.994A>G	NP_000479.1:p.Thr332Ala
XM_005245198.2:c.850A>G	XP_005245255.1:p.Thr284Ala
NM_001365052.1:c.850A>G	NP_001351981.1:p.Thr284Ala
NM_000488.4:c.994A>G MANE Select	NP_000479.1:p.Thr332Ala
NM_001365052.2:c.850A>G	NP_001351981.1:p.Thr284Ala
NM_001386302.1:c.1117A>G	NP_001373231.1:p.Thr373Ala
NM_001386303.1:c.1075A>G	NP_001373232.1:p.Thr359Ala
NM_001386304.1:c.973A>G	NP_001373233.1:p.Thr325Ala
NM_001386305.1:c.937A>G	NP_001373234.1:p.Thr313Ala
NM_001386306.1:c.778A>G	NP_001373235.1:p.Thr260Ala