Canonical Allele Identifier: CA353673156

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93619690G>C (hg19) ; chr3:g.93900846G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900846G>C , CM000665.2:g.93900846G>C	GRCh38
NC_000003.11:g.93619690G>C , CM000665.1:g.93619690G>C	GRCh37
NC_000003.10:g.95102380G>C	NCBI36
NG_009813.1:g.78245C>G , LRG_572:g.78245C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.685C>G	ENSP00000330021.7:p.Pro229Ala
ENST00000394236.9:c.685C>G MANE Select	ENSP00000377783.3:p.Pro229Ala
ENST00000407433.6:c.640C>G	ENSP00000385794.2:p.Pro214Ala
ENST00000647936.1:c.685C>G	ENSP00000496822.1:p.Pro229Ala
ENST00000648381.1:n.853C>G
ENST00000648853.1:c.643C>G	ENSP00000497262.1:p.Pro215Ala
ENST00000649103.1:c.784C>G	ENSP00000497962.1:n.784C>G
ENST00000650591.1:c.781C>G	ENSP00000497376.1:p.Pro261Ala
ENST00000394236.7:c.685C>G	ENSP00000377783.3:p.Pro229Ala
ENST00000407433.5:c.292C>G	ENSP00000385794.1:p.Pro98Ala
NM_000313.3:c.685C>G , LRG_572t1:c.685C>G	NP_000304.2:p.Pro229Ala
NM_001314077.1:c.781C>G , LRG_572t2:c.781C>G	NP_001301006.1:p.Pro261Ala
NM_000313.4:c.685C>G MANE Select	NP_000304.2:p.Pro229Ala
NM_001314077.2:c.781C>G	NP_001301006.1:p.Pro261Ala