Canonical Allele Identifier: CA343774187

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878908G>C (hg19) ; chr1:g.173909770G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909770G>C , CM000663.2:g.173909770G>C	GRCh38
NC_000001.10:g.173878908G>C , CM000663.1:g.173878908G>C	GRCh37
NC_000001.9:g.172145531G>C	NCBI36
NG_012462.1:g.12609C>G , LRG_577:g.12609C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.935C>G MANE Select	ENSP00000356671.3:p.Thr312Ser
ENST00000367698.3:c.935C>G	ENSP00000356671.3:p.Thr312Ser
ENST00000487183.1:n.586C>G
ENST00000617423.4:c.559+2094C>G	ENSP00000478688.1:n.559+2094C>G
NM_000488.3:c.935C>G , LRG_577t1:c.935C>G	NP_000479.1:p.Thr312Ser
XM_005245198.2:c.791C>G	XP_005245255.1:p.Thr264Ser
NM_001365052.1:c.791C>G	NP_001351981.1:p.Thr264Ser
NM_000488.4:c.935C>G MANE Select	NP_000479.1:p.Thr312Ser
NM_001365052.2:c.791C>G	NP_001351981.1:p.Thr264Ser
NM_001386302.1:c.1058C>G	NP_001373231.1:p.Thr353Ser
NM_001386303.1:c.1016C>G	NP_001373232.1:p.Thr339Ser
NM_001386304.1:c.914C>G	NP_001373233.1:p.Thr305Ser
NM_001386305.1:c.878C>G	NP_001373234.1:p.Thr293Ser
NM_001386306.1:c.719C>G	NP_001373235.1:p.Thr240Ser