Canonical Allele Identifier: CA353672732

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615523A>G (hg19) ; chr3:g.93896679A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896679A>G , CM000665.2:g.93896679A>G	GRCh38
NC_000003.11:g.93615523A>G , CM000665.1:g.93615523A>G	GRCh37
NC_000003.10:g.95098213A>G	NCBI36
NG_009813.1:g.82412T>C , LRG_572:g.82412T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.862T>C	ENSP00000330021.7:p.Cys288Arg
ENST00000394236.9:c.862T>C MANE Select	ENSP00000377783.3:p.Cys288Arg
ENST00000407433.6:c.817T>C	ENSP00000385794.2:p.Cys273Arg
ENST00000647936.1:c.862T>C	ENSP00000496822.1:p.Cys288Arg
ENST00000648381.1:n.1030T>C
ENST00000648853.1:c.820T>C	ENSP00000497262.1:p.Cys274Arg
ENST00000649103.1:c.961T>C	ENSP00000497962.1:n.961T>C
ENST00000650591.1:c.958T>C	ENSP00000497376.1:p.Cys320Arg
ENST00000394236.7:c.862T>C	ENSP00000377783.3:p.Cys288Arg
ENST00000407433.5:c.469T>C	ENSP00000385794.1:p.Cys157Arg
NM_000313.3:c.862T>C , LRG_572t1:c.862T>C	NP_000304.2:p.Cys288Arg
NM_001314077.1:c.958T>C , LRG_572t2:c.958T>C	NP_001301006.1:p.Cys320Arg
NM_000313.4:c.862T>C MANE Select	NP_000304.2:p.Cys288Arg
NM_001314077.2:c.958T>C	NP_001301006.1:p.Cys320Arg