Canonical Allele Identifier: CA353672974

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93617383G>C (hg19) ; chr3:g.93898539G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898539G>C , CM000665.2:g.93898539G>C	GRCh38
NC_000003.11:g.93617383G>C , CM000665.1:g.93617383G>C	GRCh37
NC_000003.10:g.95100073G>C	NCBI36
NG_009813.1:g.80552C>G , LRG_572:g.80552C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.758C>G	ENSP00000330021.7:p.Ala253Gly
ENST00000394236.9:c.758C>G MANE Select	ENSP00000377783.3:p.Ala253Gly
ENST00000407433.6:c.713C>G	ENSP00000385794.2:p.Ala238Gly
ENST00000647936.1:c.758C>G	ENSP00000496822.1:p.Ala253Gly
ENST00000648381.1:n.926C>G
ENST00000648853.1:c.716C>G	ENSP00000497262.1:p.Ala239Gly
ENST00000649103.1:c.857C>G	ENSP00000497962.1:n.857C>G
ENST00000650591.1:c.854C>G	ENSP00000497376.1:p.Ala285Gly
ENST00000394236.7:c.758C>G	ENSP00000377783.3:p.Ala253Gly
ENST00000407433.5:c.365C>G	ENSP00000385794.1:p.Ala122Gly
NM_000313.3:c.758C>G , LRG_572t1:c.758C>G	NP_000304.2:p.Ala253Gly
NM_001314077.1:c.854C>G , LRG_572t2:c.854C>G	NP_001301006.1:p.Ala285Gly
NM_000313.4:c.758C>G MANE Select	NP_000304.2:p.Ala253Gly
NM_001314077.2:c.854C>G	NP_001301006.1:p.Ala285Gly