Canonical Allele Identifier: CA434460818

Gene: PROS1

Linked Data

• gnomAD v4: 3-93896587-T-C
• MyVariant Identifiers: chr3:g.93615431T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896587T>C , CM000665.2:g.93896587T>C	GRCh38
NC_000003.11:g.93615431T>C , CM000665.1:g.93615431T>C	GRCh37
NC_000003.10:g.95098121T>C	NCBI36
NG_009813.1:g.82504A>G , LRG_572:g.82504A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.954A>G	ENSP00000330021.7:p.Pro318=
ENST00000394236.9:c.954A>G MANE Select	ENSP00000377783.3:p.Pro318=
ENST00000407433.6:c.909A>G	ENSP00000385794.2:p.Pro303=
ENST00000647936.1:c.954A>G	ENSP00000496822.1:p.Pro318=
ENST00000648381.1:n.1122A>G
ENST00000648853.1:c.912A>G	ENSP00000497262.1:p.Pro304=
ENST00000649103.1:c.1053A>G	ENSP00000497962.1:n.1053A>G
ENST00000650591.1:c.1050A>G	ENSP00000497376.1:p.Pro350=
ENST00000394236.7:c.954A>G	ENSP00000377783.3:p.Pro318=
ENST00000407433.5:c.561A>G	ENSP00000385794.1:p.Pro187=
NM_000313.3:c.954A>G , LRG_572t1:c.954A>G	NP_000304.2:p.Pro318=
NM_001314077.1:c.1050A>G , LRG_572t2:c.1050A>G	NP_001301006.1:p.Pro350=
NM_000313.4:c.954A>G MANE Select	NP_000304.2:p.Pro318=
NM_001314077.2:c.1050A>G	NP_001301006.1:p.Pro350=