Canonical Allele Identifier: CA353672144

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598131T>G (hg19) ; chr3:g.93879287T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879287T>G , CM000665.2:g.93879287T>G	GRCh38
NC_000003.11:g.93598131T>G , CM000665.1:g.93598131T>G	GRCh37
NC_000003.10:g.95080821T>G	NCBI36
NG_009813.1:g.99804A>C , LRG_572:g.99804A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1520A>C	ENSP00000330021.7:p.His507Pro
ENST00000394236.9:c.1520A>C MANE Select	ENSP00000377783.3:p.His507Pro
ENST00000407433.6:c.1475A>C	ENSP00000385794.2:p.His492Pro
ENST00000647936.1:c.1520A>C	ENSP00000496822.1:p.His507Pro
ENST00000648381.1:n.1688A>C
ENST00000648853.1:c.1478A>C	ENSP00000497262.1:p.His493Pro
ENST00000649103.1:c.1619A>C	ENSP00000497962.1:n.1619A>C
ENST00000649585.1:c.463A>C	ENSP00000498163.1:n.463A>C
ENST00000650591.1:c.1616A>C	ENSP00000497376.1:p.His539Pro
ENST00000394236.7:c.1520A>C	ENSP00000377783.3:p.His507Pro
ENST00000407433.5:c.1127A>C	ENSP00000385794.1:p.His376Pro
NM_000313.3:c.1520A>C , LRG_572t1:c.1520A>C	NP_000304.2:p.His507Pro
NM_001314077.1:c.1616A>C , LRG_572t2:c.1616A>C	NP_001301006.1:p.His539Pro
NM_000313.4:c.1520A>C MANE Select	NP_000304.2:p.His507Pro
NM_001314077.2:c.1616A>C	NP_001301006.1:p.His539Pro