Canonical Allele Identifier: CA353674595

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646177G>T (hg19) ; chr3:g.93927333G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927333G>T , CM000665.2:g.93927333G>T	GRCh38
NC_000003.11:g.93646177G>T , CM000665.1:g.93646177G>T	GRCh37
NC_000003.10:g.95128867G>T	NCBI36
NG_009813.1:g.51758C>A , LRG_572:g.51758C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.151C>A	ENSP00000330021.7:p.Gln51Lys
ENST00000394236.9:c.151C>A MANE Select	ENSP00000377783.3:p.Gln51Lys
ENST00000407433.6:c.151C>A	ENSP00000385794.2:p.Gln51Lys
ENST00000472684.2:c.-243C>A	ENSP00000419616.2:n.-243C>A
ENST00000647936.1:c.151C>A	ENSP00000496822.1:p.Gln51Lys
ENST00000648381.1:n.319C>A
ENST00000648853.1:c.109C>A	ENSP00000497262.1:p.Gln37Lys
ENST00000649103.1:c.130C>A	ENSP00000497962.1:p.Gln44Lys
ENST00000650591.1:c.247C>A	ENSP00000497376.1:p.Gln83Lys
ENST00000348974.4:c.247C>A	ENSP00000330021.6:p.Gln83Lys
ENST00000394236.7:c.151C>A	ENSP00000377783.3:p.Gln51Lys
ENST00000407433.5:c.-243C>A	ENSP00000385794.1:n.-243C>A
ENST00000472684.1:c.-243C>A	ENSP00000419616.1:n.-243C>A
NM_000313.3:c.151C>A , LRG_572t1:c.151C>A	NP_000304.2:p.Gln51Lys
NM_001314077.1:c.247C>A , LRG_572t2:c.247C>A	NP_001301006.1:p.Gln83Lys
NM_000313.4:c.151C>A MANE Select	NP_000304.2:p.Gln51Lys
NM_001314077.2:c.247C>A	NP_001301006.1:p.Gln83Lys