Canonical Allele Identifier: CA434460843

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615464T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896620T>G , CM000665.2:g.93896620T>G	GRCh38
NC_000003.11:g.93615464T>G , CM000665.1:g.93615464T>G	GRCh37
NC_000003.10:g.95098154T>G	NCBI36
NG_009813.1:g.82471A>C , LRG_572:g.82471A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.921A>C	ENSP00000330021.7:p.Ala307=
ENST00000394236.9:c.921A>C MANE Select	ENSP00000377783.3:p.Ala307=
ENST00000407433.6:c.876A>C	ENSP00000385794.2:p.Ala292=
ENST00000647936.1:c.921A>C	ENSP00000496822.1:p.Ala307=
ENST00000648381.1:n.1089A>C
ENST00000648853.1:c.879A>C	ENSP00000497262.1:p.Ala293=
ENST00000649103.1:c.1020A>C	ENSP00000497962.1:n.1020A>C
ENST00000650591.1:c.1017A>C	ENSP00000497376.1:p.Ala339=
ENST00000394236.7:c.921A>C	ENSP00000377783.3:p.Ala307=
ENST00000407433.5:c.528A>C	ENSP00000385794.1:p.Ala176=
NM_000313.3:c.921A>C , LRG_572t1:c.921A>C	NP_000304.2:p.Ala307=
NM_001314077.1:c.1017A>C , LRG_572t2:c.1017A>C	NP_001301006.1:p.Ala339=
NM_000313.4:c.921A>C MANE Select	NP_000304.2:p.Ala307=
NM_001314077.2:c.1017A>C	NP_001301006.1:p.Ala339=