Canonical Allele Identifier: CA353672613

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615471T>G (hg19) ; chr3:g.93896627T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896627T>G , CM000665.2:g.93896627T>G	GRCh38
NC_000003.11:g.93615471T>G , CM000665.1:g.93615471T>G	GRCh37
NC_000003.10:g.95098161T>G	NCBI36
NG_009813.1:g.82464A>C , LRG_572:g.82464A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.914A>C	ENSP00000330021.7:p.Gln305Pro
ENST00000394236.9:c.914A>C MANE Select	ENSP00000377783.3:p.Gln305Pro
ENST00000407433.6:c.869A>C	ENSP00000385794.2:p.Gln290Pro
ENST00000647936.1:c.914A>C	ENSP00000496822.1:p.Gln305Pro
ENST00000648381.1:n.1082A>C
ENST00000648853.1:c.872A>C	ENSP00000497262.1:p.Gln291Pro
ENST00000649103.1:c.1013A>C	ENSP00000497962.1:n.1013A>C
ENST00000650591.1:c.1010A>C	ENSP00000497376.1:p.Gln337Pro
ENST00000394236.7:c.914A>C	ENSP00000377783.3:p.Gln305Pro
ENST00000407433.5:c.521A>C	ENSP00000385794.1:p.Gln174Pro
NM_000313.3:c.914A>C , LRG_572t1:c.914A>C	NP_000304.2:p.Gln305Pro
NM_001314077.1:c.1010A>C , LRG_572t2:c.1010A>C	NP_001301006.1:p.Gln337Pro
NM_000313.4:c.914A>C MANE Select	NP_000304.2:p.Gln305Pro
NM_001314077.2:c.1010A>C	NP_001301006.1:p.Gln337Pro