Canonical Allele Identifier: CA343774548

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878993T>C (hg19) ; chr1:g.173909855T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909855T>C , CM000663.2:g.173909855T>C	GRCh38
NC_000001.10:g.173878993T>C , CM000663.1:g.173878993T>C	GRCh37
NC_000001.9:g.172145616T>C	NCBI36
NG_012462.1:g.12524A>G , LRG_577:g.12524A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.850A>G MANE Select	ENSP00000356671.3:p.Met284Val
ENST00000367698.3:c.850A>G	ENSP00000356671.3:p.Met284Val
ENST00000487183.1:n.501A>G
ENST00000617423.4:c.559+2009A>G	ENSP00000478688.1:n.559+2009A>G
NM_000488.3:c.850A>G , LRG_577t1:c.850A>G	NP_000479.1:p.Met284Val
XM_005245198.2:c.706A>G	XP_005245255.1:p.Met236Val
NM_001365052.1:c.706A>G	NP_001351981.1:p.Met236Val
NM_000488.4:c.850A>G MANE Select	NP_000479.1:p.Met284Val
NM_001365052.2:c.706A>G	NP_001351981.1:p.Met236Val
NM_001386302.1:c.973A>G	NP_001373231.1:p.Met325Val
NM_001386303.1:c.931A>G	NP_001373232.1:p.Met311Val
NM_001386304.1:c.829A>G	NP_001373233.1:p.Met277Val
NM_001386305.1:c.793A>G	NP_001373234.1:p.Met265Val
NM_001386306.1:c.634A>G	NP_001373235.1:p.Met212Val