Canonical Allele Identifier: CA353672741

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615529A>C (hg19) ; chr3:g.93896685A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896685A>C , CM000665.2:g.93896685A>C	GRCh38
NC_000003.11:g.93615529A>C , CM000665.1:g.93615529A>C	GRCh37
NC_000003.10:g.95098219A>C	NCBI36
NG_009813.1:g.82406T>G , LRG_572:g.82406T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.856T>G	ENSP00000330021.7:p.Ser286Ala
ENST00000394236.9:c.856T>G MANE Select	ENSP00000377783.3:p.Ser286Ala
ENST00000407433.6:c.811T>G	ENSP00000385794.2:p.Ser271Ala
ENST00000647936.1:c.856T>G	ENSP00000496822.1:p.Ser286Ala
ENST00000648381.1:n.1024T>G
ENST00000648853.1:c.814T>G	ENSP00000497262.1:p.Ser272Ala
ENST00000649103.1:c.955T>G	ENSP00000497962.1:n.955T>G
ENST00000650591.1:c.952T>G	ENSP00000497376.1:p.Ser318Ala
ENST00000394236.7:c.856T>G	ENSP00000377783.3:p.Ser286Ala
ENST00000407433.5:c.463T>G	ENSP00000385794.1:p.Ser155Ala
NM_000313.3:c.856T>G , LRG_572t1:c.856T>G	NP_000304.2:p.Ser286Ala
NM_001314077.1:c.952T>G , LRG_572t2:c.952T>G	NP_001301006.1:p.Ser318Ala
NM_000313.4:c.856T>G MANE Select	NP_000304.2:p.Ser286Ala
NM_001314077.2:c.952T>G	NP_001301006.1:p.Ser318Ala