Canonical Allele Identifier: CA353672736

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615526C>T (hg19) ; chr3:g.93896682C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896682C>T , CM000665.2:g.93896682C>T	GRCh38
NC_000003.11:g.93615526C>T , CM000665.1:g.93615526C>T	GRCh37
NC_000003.10:g.95098216C>T	NCBI36
NG_009813.1:g.82409G>A , LRG_572:g.82409G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.859G>A	ENSP00000330021.7:p.Val287Met
ENST00000394236.9:c.859G>A MANE Select	ENSP00000377783.3:p.Val287Met
ENST00000407433.6:c.814G>A	ENSP00000385794.2:p.Val272Met
ENST00000647936.1:c.859G>A	ENSP00000496822.1:p.Val287Met
ENST00000648381.1:n.1027G>A
ENST00000648853.1:c.817G>A	ENSP00000497262.1:p.Val273Met
ENST00000649103.1:c.958G>A	ENSP00000497962.1:n.958G>A
ENST00000650591.1:c.955G>A	ENSP00000497376.1:p.Val319Met
ENST00000394236.7:c.859G>A	ENSP00000377783.3:p.Val287Met
ENST00000407433.5:c.466G>A	ENSP00000385794.1:p.Val156Met
NM_000313.3:c.859G>A , LRG_572t1:c.859G>A	NP_000304.2:p.Val287Met
NM_001314077.1:c.955G>A , LRG_572t2:c.955G>A	NP_001301006.1:p.Val319Met
NM_000313.4:c.859G>A MANE Select	NP_000304.2:p.Val287Met
NM_001314077.2:c.955G>A	NP_001301006.1:p.Val319Met