Canonical Allele Identifier: CA353672132

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598128A>C (hg19) ; chr3:g.93879284A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879284A>C , CM000665.2:g.93879284A>C	GRCh38
NC_000003.11:g.93598128A>C , CM000665.1:g.93598128A>C	GRCh37
NC_000003.10:g.95080818A>C	NCBI36
NG_009813.1:g.99807T>G , LRG_572:g.99807T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1523T>G	ENSP00000330021.7:p.Val508Gly
ENST00000394236.9:c.1523T>G MANE Select	ENSP00000377783.3:p.Val508Gly
ENST00000407433.6:c.1478T>G	ENSP00000385794.2:p.Val493Gly
ENST00000647936.1:c.1523T>G	ENSP00000496822.1:p.Val508Gly
ENST00000648381.1:n.1691T>G
ENST00000648853.1:c.1481T>G	ENSP00000497262.1:p.Val494Gly
ENST00000649103.1:c.1622T>G	ENSP00000497962.1:n.1622T>G
ENST00000649585.1:c.466T>G	ENSP00000498163.1:n.466T>G
ENST00000650591.1:c.1619T>G	ENSP00000497376.1:p.Val540Gly
ENST00000394236.7:c.1523T>G	ENSP00000377783.3:p.Val508Gly
ENST00000407433.5:c.1130T>G	ENSP00000385794.1:p.Val377Gly
NM_000313.3:c.1523T>G , LRG_572t1:c.1523T>G	NP_000304.2:p.Val508Gly
NM_001314077.1:c.1619T>G , LRG_572t2:c.1619T>G	NP_001301006.1:p.Val540Gly
NM_000313.4:c.1523T>G MANE Select	NP_000304.2:p.Val508Gly
NM_001314077.2:c.1619T>G	NP_001301006.1:p.Val540Gly