Canonical Allele Identifier: CA353672587

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615459A>G (hg19) ; chr3:g.93896615A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896615A>G , CM000665.2:g.93896615A>G	GRCh38
NC_000003.11:g.93615459A>G , CM000665.1:g.93615459A>G	GRCh37
NC_000003.10:g.95098149A>G	NCBI36
NG_009813.1:g.82476T>C , LRG_572:g.82476T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.926T>C	ENSP00000330021.7:p.Val309Ala
ENST00000394236.9:c.926T>C MANE Select	ENSP00000377783.3:p.Val309Ala
ENST00000407433.6:c.881T>C	ENSP00000385794.2:p.Val294Ala
ENST00000647936.1:c.926T>C	ENSP00000496822.1:p.Val309Ala
ENST00000648381.1:n.1094T>C
ENST00000648853.1:c.884T>C	ENSP00000497262.1:p.Val295Ala
ENST00000649103.1:c.1025T>C	ENSP00000497962.1:n.1025T>C
ENST00000650591.1:c.1022T>C	ENSP00000497376.1:p.Val341Ala
ENST00000394236.7:c.926T>C	ENSP00000377783.3:p.Val309Ala
ENST00000407433.5:c.533T>C	ENSP00000385794.1:p.Val178Ala
NM_000313.3:c.926T>C , LRG_572t1:c.926T>C	NP_000304.2:p.Val309Ala
NM_001314077.1:c.1022T>C , LRG_572t2:c.1022T>C	NP_001301006.1:p.Val341Ala
NM_000313.4:c.926T>C MANE Select	NP_000304.2:p.Val309Ala
NM_001314077.2:c.1022T>C	NP_001301006.1:p.Val341Ala