Canonical Allele Identifier: CA4731353

Gene: PLAT

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42187447G>T , CM000670.2:g.42187447G>T	GRCh38
NC_000008.10:g.42044965G>T , CM000670.1:g.42044965G>T	GRCh37
NC_000008.9:g.42164122G>T	NCBI36
NG_023264.1:g.25230C>A , LRG_570:g.25230C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220809.9:c.490C>A MANE Select	ENSP00000220809.4:p.Arg164=
ENST00000677722.1:n.732C>A
ENST00000678083.1:c.490C>A	ENSP00000504824.1:p.Arg164=
ENST00000678676.1:c.490C>A	ENSP00000502858.1:p.Arg164=
ENST00000679151.1:c.490C>A	ENSP00000504311.1:p.Arg164=
ENST00000679300.1:c.490C>A	ENSP00000503050.1:p.Arg164=
ENST00000220809.8:c.490C>A	ENSP00000220809.4:p.Arg164=
ENST00000352041.7:c.352C>A	ENSP00000270188.6:p.Arg118=
ENST00000429089.6:c.490C>A	ENSP00000392045.2:p.Arg164=
ENST00000429710.6:c.253+1487C>A	ENSP00000407861.2:n.253+1487C>A
ENST00000519510.5:c.364+459C>A	ENSP00000428886.1:n.364+459C>A
ENST00000520523.5:c.490C>A	ENSP00000428797.1:p.Arg164=
ENST00000521042.1:c.153C>A
ENST00000521647.1:n.710C>A
ENST00000524009.5:c.364+459C>A	ENSP00000429401.1:n.364+459C>A
NM_000930.3:c.490C>A , LRG_570t1:c.490C>A	NP_000921.1:p.Arg164=
NM_033011.2:c.352C>A	NP_127509.1:p.Arg118=
NM_000930.4:c.490C>A	NP_000921.1:p.Arg164=
NM_001319189.1:c.364+459C>A	NP_001306118.1:n.364+459C>A
NM_033011.3:c.352C>A	NP_127509.1:p.Arg118=
NM_000930.5:c.490C>A MANE Select	NP_000921.1:p.Arg164=
NM_001319189.2:c.364+459C>A	NP_001306118.1:n.364+459C>A
NM_033011.4:c.352C>A	NP_127509.1:p.Arg118=