Canonical Allele Identifier: CA353672571

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615451A>C (hg19) ; chr3:g.93896607A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896607A>C , CM000665.2:g.93896607A>C	GRCh38
NC_000003.11:g.93615451A>C , CM000665.1:g.93615451A>C	GRCh37
NC_000003.10:g.95098141A>C	NCBI36
NG_009813.1:g.82484T>G , LRG_572:g.82484T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.934T>G	ENSP00000330021.7:p.Tyr312Asp
ENST00000394236.9:c.934T>G MANE Select	ENSP00000377783.3:p.Tyr312Asp
ENST00000407433.6:c.889T>G	ENSP00000385794.2:p.Tyr297Asp
ENST00000647936.1:c.934T>G	ENSP00000496822.1:p.Tyr312Asp
ENST00000648381.1:n.1102T>G
ENST00000648853.1:c.892T>G	ENSP00000497262.1:p.Tyr298Asp
ENST00000649103.1:c.1033T>G	ENSP00000497962.1:n.1033T>G
ENST00000650591.1:c.1030T>G	ENSP00000497376.1:p.Tyr344Asp
ENST00000394236.7:c.934T>G	ENSP00000377783.3:p.Tyr312Asp
ENST00000407433.5:c.541T>G	ENSP00000385794.1:p.Tyr181Asp
NM_000313.3:c.934T>G , LRG_572t1:c.934T>G	NP_000304.2:p.Tyr312Asp
NM_001314077.1:c.1030T>G , LRG_572t2:c.1030T>G	NP_001301006.1:p.Tyr344Asp
NM_000313.4:c.934T>G MANE Select	NP_000304.2:p.Tyr312Asp
NM_001314077.2:c.1030T>G	NP_001301006.1:p.Tyr344Asp