Canonical Allele Identifier: CA353674683

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646221A>T (hg19) ; chr3:g.93927377A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927377A>T , CM000665.2:g.93927377A>T	GRCh38
NC_000003.11:g.93646221A>T , CM000665.1:g.93646221A>T	GRCh37
NC_000003.10:g.95128911A>T	NCBI36
NG_009813.1:g.51714T>A , LRG_572:g.51714T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.107T>A	ENSP00000330021.7:p.Leu36Gln
ENST00000394236.9:c.107T>A MANE Select	ENSP00000377783.3:p.Leu36Gln
ENST00000407433.6:c.107T>A	ENSP00000385794.2:p.Leu36Gln
ENST00000472684.2:c.-287T>A	ENSP00000419616.2:n.-287T>A
ENST00000647936.1:c.107T>A	ENSP00000496822.1:p.Leu36Gln
ENST00000648381.1:n.275T>A
ENST00000648853.1:c.65T>A	ENSP00000497262.1:p.Leu22Gln
ENST00000649103.1:c.86T>A	ENSP00000497962.1:p.Leu29Gln
ENST00000650591.1:c.203T>A	ENSP00000497376.1:p.Leu68Gln
ENST00000348974.4:c.203T>A	ENSP00000330021.6:p.Leu68Gln
ENST00000394236.7:c.107T>A	ENSP00000377783.3:p.Leu36Gln
ENST00000407433.5:c.-287T>A	ENSP00000385794.1:n.-287T>A
ENST00000472684.1:c.-287T>A	ENSP00000419616.1:n.-287T>A
NM_000313.3:c.107T>A , LRG_572t1:c.107T>A	NP_000304.2:p.Leu36Gln
NM_001314077.1:c.203T>A , LRG_572t2:c.203T>A	NP_001301006.1:p.Leu68Gln
NM_000313.4:c.107T>A MANE Select	NP_000304.2:p.Leu36Gln
NM_001314077.2:c.203T>A	NP_001301006.1:p.Leu68Gln