Canonical Allele Identifier: CA434462779

Gene: PROS1

Linked Data

• gnomAD v4: 3-93927256-C-G
• MyVariant Identifiers: chr3:g.93646100C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927256C>G , CM000665.2:g.93927256C>G	GRCh38
NC_000003.11:g.93646100C>G , CM000665.1:g.93646100C>G	GRCh37
NC_000003.10:g.95128790C>G	NCBI36
NG_009813.1:g.51835G>C , LRG_572:g.51835G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.228G>C	ENSP00000330021.7:p.Pro76=
ENST00000394236.9:c.228G>C MANE Select	ENSP00000377783.3:p.Pro76=
ENST00000407433.6:c.228G>C	ENSP00000385794.2:p.Pro76=
ENST00000472684.2:c.-166G>C	ENSP00000419616.2:n.-166G>C
ENST00000647936.1:c.228G>C	ENSP00000496822.1:p.Pro76=
ENST00000648381.1:n.396G>C
ENST00000648853.1:c.186G>C	ENSP00000497262.1:p.Pro62=
ENST00000649103.1:c.207G>C	ENSP00000497962.1:p.Pro69=
ENST00000650591.1:c.324G>C	ENSP00000497376.1:p.Pro108=
ENST00000348974.4:c.324G>C	ENSP00000330021.6:p.Pro108=
ENST00000394236.7:c.228G>C	ENSP00000377783.3:p.Pro76=
ENST00000407433.5:c.-166G>C	ENSP00000385794.1:n.-166G>C
ENST00000472684.1:c.-166G>C	ENSP00000419616.1:n.-166G>C
NM_000313.3:c.228G>C , LRG_572t1:c.228G>C	NP_000304.2:p.Pro76=
NM_001314077.1:c.324G>C , LRG_572t2:c.324G>C	NP_001301006.1:p.Pro108=
NM_000313.4:c.228G>C MANE Select	NP_000304.2:p.Pro76=
NM_001314077.2:c.324G>C	NP_001301006.1:p.Pro108=