Canonical Allele Identifier: CA353669494

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593129T>G (hg19) ; chr3:g.93874285T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874285T>G , CM000665.2:g.93874285T>G	GRCh38
NC_000003.11:g.93593129T>G , CM000665.1:g.93593129T>G	GRCh37
NC_000003.10:g.95075819T>G	NCBI36
NG_009813.1:g.104806A>C , LRG_572:g.104806A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1991A>C	ENSP00000330021.7:p.His664Pro
ENST00000394236.9:c.1991A>C MANE Select	ENSP00000377783.3:p.His664Pro
ENST00000407433.6:c.1946A>C	ENSP00000385794.2:p.His649Pro
ENST00000647936.1:c.*94A>C	ENSP00000496822.1:n.*94A>C
ENST00000648381.1:n.2159A>C
ENST00000648853.1:c.1949A>C	ENSP00000497262.1:p.His650Pro
ENST00000650591.1:c.2087A>C	ENSP00000497376.1:p.His696Pro
ENST00000394236.7:c.1991A>C	ENSP00000377783.3:p.His664Pro
ENST00000407433.5:c.1598A>C	ENSP00000385794.1:p.His533Pro
NM_000313.3:c.1991A>C , LRG_572t1:c.1991A>C	NP_000304.2:p.His664Pro
NM_001314077.1:c.2087A>C , LRG_572t2:c.2087A>C	NP_001301006.1:p.His696Pro
NM_000313.4:c.1991A>C MANE Select	NP_000304.2:p.His664Pro
NM_001314077.2:c.2087A>C	NP_001301006.1:p.His696Pro