Canonical Allele Identifier: CA434460846

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615467A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896623A>G , CM000665.2:g.93896623A>G	GRCh38
NC_000003.11:g.93615467A>G , CM000665.1:g.93615467A>G	GRCh37
NC_000003.10:g.95098157A>G	NCBI36
NG_009813.1:g.82468T>C , LRG_572:g.82468T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.918T>C	ENSP00000330021.7:p.Phe306=
ENST00000394236.9:c.918T>C MANE Select	ENSP00000377783.3:p.Phe306=
ENST00000407433.6:c.873T>C	ENSP00000385794.2:p.Phe291=
ENST00000647936.1:c.918T>C	ENSP00000496822.1:p.Phe306=
ENST00000648381.1:n.1086T>C
ENST00000648853.1:c.876T>C	ENSP00000497262.1:p.Phe292=
ENST00000649103.1:c.1017T>C	ENSP00000497962.1:n.1017T>C
ENST00000650591.1:c.1014T>C	ENSP00000497376.1:p.Phe338=
ENST00000394236.7:c.918T>C	ENSP00000377783.3:p.Phe306=
ENST00000407433.5:c.525T>C	ENSP00000385794.1:p.Phe175=
NM_000313.3:c.918T>C , LRG_572t1:c.918T>C	NP_000304.2:p.Phe306=
NM_001314077.1:c.1014T>C , LRG_572t2:c.1014T>C	NP_001301006.1:p.Phe338=
NM_000313.4:c.918T>C MANE Select	NP_000304.2:p.Phe306=
NM_001314077.2:c.1014T>C	NP_001301006.1:p.Phe338=