Canonical Allele Identifier: CA353671650

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598016T>G (hg19) ; chr3:g.93879172T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879172T>G , CM000665.2:g.93879172T>G	GRCh38
NC_000003.11:g.93598016T>G , CM000665.1:g.93598016T>G	GRCh37
NC_000003.10:g.95080706T>G	NCBI36
NG_009813.1:g.99919A>C , LRG_572:g.99919A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1635A>C	ENSP00000330021.7:p.Glu545Asp
ENST00000394236.9:c.1635A>C MANE Select	ENSP00000377783.3:p.Glu545Asp
ENST00000407433.6:c.1590A>C	ENSP00000385794.2:p.Glu530Asp
ENST00000647936.1:c.1635A>C	ENSP00000496822.1:p.Glu545Asp
ENST00000648381.1:n.1803A>C
ENST00000648853.1:c.1593A>C	ENSP00000497262.1:p.Glu531Asp
ENST00000649103.1:c.1734A>C	ENSP00000497962.1:n.1734A>C
ENST00000649585.1:c.578A>C	ENSP00000498163.1:n.578A>C
ENST00000650591.1:c.1731A>C	ENSP00000497376.1:p.Glu577Asp
ENST00000394236.7:c.1635A>C	ENSP00000377783.3:p.Glu545Asp
ENST00000407433.5:c.1242A>C	ENSP00000385794.1:p.Glu414Asp
NM_000313.3:c.1635A>C , LRG_572t1:c.1635A>C	NP_000304.2:p.Glu545Asp
NM_001314077.1:c.1731A>C , LRG_572t2:c.1731A>C	NP_001301006.1:p.Glu577Asp
NM_000313.4:c.1635A>C MANE Select	NP_000304.2:p.Glu545Asp
NM_001314077.2:c.1731A>C	NP_001301006.1:p.Glu577Asp