Canonical Allele Identifier: CA353673140

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93619683C>A (hg19) ; chr3:g.93900839C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900839C>A , CM000665.2:g.93900839C>A	GRCh38
NC_000003.11:g.93619683C>A , CM000665.1:g.93619683C>A	GRCh37
NC_000003.10:g.95102373C>A	NCBI36
NG_009813.1:g.78252G>T , LRG_572:g.78252G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.692G>T	ENSP00000330021.7:p.Gly231Val
ENST00000394236.9:c.692G>T MANE Select	ENSP00000377783.3:p.Gly231Val
ENST00000407433.6:c.647G>T	ENSP00000385794.2:p.Gly216Val
ENST00000647936.1:c.692G>T	ENSP00000496822.1:p.Gly231Val
ENST00000648381.1:n.860G>T
ENST00000648853.1:c.650G>T	ENSP00000497262.1:p.Gly217Val
ENST00000649103.1:c.791G>T	ENSP00000497962.1:n.791G>T
ENST00000650591.1:c.788G>T	ENSP00000497376.1:p.Gly263Val
ENST00000394236.7:c.692G>T	ENSP00000377783.3:p.Gly231Val
ENST00000407433.5:c.299G>T	ENSP00000385794.1:p.Gly100Val
NM_000313.3:c.692G>T , LRG_572t1:c.692G>T	NP_000304.2:p.Gly231Val
NM_001314077.1:c.788G>T , LRG_572t2:c.788G>T	NP_001301006.1:p.Gly263Val
NM_000313.4:c.692G>T MANE Select	NP_000304.2:p.Gly231Val
NM_001314077.2:c.788G>T	NP_001301006.1:p.Gly263Val