Canonical Allele Identifier: CA434462848

Gene: PROS1

Linked Data

• gnomAD v3: 3-93927328-A-G
• gnomAD v4: 3-93927328-A-G
• MyVariant Identifiers: chr3:g.93646172A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927328A>G , CM000665.2:g.93927328A>G	GRCh38
NC_000003.11:g.93646172A>G , CM000665.1:g.93646172A>G	GRCh37
NC_000003.10:g.95128862A>G	NCBI36
NG_009813.1:g.51763T>C , LRG_572:g.51763T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.156T>C	ENSP00000330021.7:p.Gly52=
ENST00000394236.9:c.156T>C MANE Select	ENSP00000377783.3:p.Gly52=
ENST00000407433.6:c.156T>C	ENSP00000385794.2:p.Gly52=
ENST00000472684.2:c.-238T>C	ENSP00000419616.2:n.-238T>C
ENST00000647936.1:c.156T>C	ENSP00000496822.1:p.Gly52=
ENST00000648381.1:n.324T>C
ENST00000648853.1:c.114T>C	ENSP00000497262.1:p.Gly38=
ENST00000649103.1:c.135T>C	ENSP00000497962.1:p.Gly45=
ENST00000650591.1:c.252T>C	ENSP00000497376.1:p.Gly84=
ENST00000348974.4:c.252T>C	ENSP00000330021.6:p.Gly84=
ENST00000394236.7:c.156T>C	ENSP00000377783.3:p.Gly52=
ENST00000407433.5:c.-238T>C	ENSP00000385794.1:n.-238T>C
ENST00000472684.1:c.-238T>C	ENSP00000419616.1:n.-238T>C
NM_000313.3:c.156T>C , LRG_572t1:c.156T>C	NP_000304.2:p.Gly52=
NM_001314077.1:c.252T>C , LRG_572t2:c.252T>C	NP_001301006.1:p.Gly84=
NM_000313.4:c.156T>C MANE Select	NP_000304.2:p.Gly52=
NM_001314077.2:c.252T>C	NP_001301006.1:p.Gly84=