Canonical Allele Identifier: CA353672692

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615505C>G (hg19) ; chr3:g.93896661C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896661C>G , CM000665.2:g.93896661C>G	GRCh38
NC_000003.11:g.93615505C>G , CM000665.1:g.93615505C>G	GRCh37
NC_000003.10:g.95098195C>G	NCBI36
NG_009813.1:g.82430G>C , LRG_572:g.82430G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.880G>C	ENSP00000330021.7:p.Asp294His
ENST00000394236.9:c.880G>C MANE Select	ENSP00000377783.3:p.Asp294His
ENST00000407433.6:c.835G>C	ENSP00000385794.2:p.Asp279His
ENST00000647936.1:c.880G>C	ENSP00000496822.1:p.Asp294His
ENST00000648381.1:n.1048G>C
ENST00000648853.1:c.838G>C	ENSP00000497262.1:p.Asp280His
ENST00000649103.1:c.979G>C	ENSP00000497962.1:n.979G>C
ENST00000650591.1:c.976G>C	ENSP00000497376.1:p.Asp326His
ENST00000394236.7:c.880G>C	ENSP00000377783.3:p.Asp294His
ENST00000407433.5:c.487G>C	ENSP00000385794.1:p.Asp163His
NM_000313.3:c.880G>C , LRG_572t1:c.880G>C	NP_000304.2:p.Asp294His
NM_001314077.1:c.976G>C , LRG_572t2:c.976G>C	NP_001301006.1:p.Asp326His
NM_000313.4:c.880G>C MANE Select	NP_000304.2:p.Asp294His
NM_001314077.2:c.976G>C	NP_001301006.1:p.Asp326His