Canonical Allele Identifier: CA434460873

Gene: PROS1

Linked Data

• gnomAD v4: 3-93896671-G-C
• MyVariant Identifiers: chr3:g.93615515G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896671G>C , CM000665.2:g.93896671G>C	GRCh38
NC_000003.11:g.93615515G>C , CM000665.1:g.93615515G>C	GRCh37
NC_000003.10:g.95098205G>C	NCBI36
NG_009813.1:g.82420C>G , LRG_572:g.82420C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.870C>G	ENSP00000330021.7:p.Pro290=
ENST00000394236.9:c.870C>G MANE Select	ENSP00000377783.3:p.Pro290=
ENST00000407433.6:c.825C>G	ENSP00000385794.2:p.Pro275=
ENST00000647936.1:c.870C>G	ENSP00000496822.1:p.Pro290=
ENST00000648381.1:n.1038C>G
ENST00000648853.1:c.828C>G	ENSP00000497262.1:p.Pro276=
ENST00000649103.1:c.969C>G	ENSP00000497962.1:n.969C>G
ENST00000650591.1:c.966C>G	ENSP00000497376.1:p.Pro322=
ENST00000394236.7:c.870C>G	ENSP00000377783.3:p.Pro290=
ENST00000407433.5:c.477C>G	ENSP00000385794.1:p.Pro159=
NM_000313.3:c.870C>G , LRG_572t1:c.870C>G	NP_000304.2:p.Pro290=
NM_001314077.1:c.966C>G , LRG_572t2:c.966C>G	NP_001301006.1:p.Pro322=
NM_000313.4:c.870C>G MANE Select	NP_000304.2:p.Pro290=
NM_001314077.2:c.966C>G	NP_001301006.1:p.Pro322=