Canonical Allele Identifier: CA1779315042

Gene: PLAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42197659A= , CM000670.2:g.42197659A=	GRCh38
NC_000008.10:g.42055177A= , CM000670.1:g.42055177A=	GRCh37
NC_000008.9:g.42174334A=	NCBI36
NG_023264.1:g.15018T= , LRG_570:g.15018T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220809.9:c.-26-4448T= MANE Select	ENSP00000220809.4:n.-26-4448T=
ENST00000677722.1:n.217-4448T=
ENST00000678676.1:c.-26-4448T=	ENSP00000502858.1:n.-26-4448T=
ENST00000679151.1:c.-47-4427T=	ENSP00000504311.1:n.-47-4427T=
ENST00000679300.1:c.-26-4448T=	ENSP00000503050.1:n.-26-4448T=
ENST00000220809.8:c.-26-4448T=	ENSP00000220809.4:n.-26-4448T=
ENST00000352041.7:c.-26-4448T=	ENSP00000270188.6:n.-26-4448T=
ENST00000429089.6:c.-26-4448T=	ENSP00000392045.2:n.-26-4448T=
ENST00000429710.6:c.-26-4448T=	ENSP00000407861.2:n.-26-4448T=
ENST00000519510.5:c.-26-4448T=	ENSP00000428886.1:n.-26-4448T=
ENST00000524009.5:c.-26-4448T=	ENSP00000429401.1:n.-26-4448T=
NM_000930.3:c.-26-4448T= , LRG_570t1:c.-26-4448T=	NP_000921.1:n.-26-4448T=
NM_033011.2:c.-26-4448T=	NP_127509.1:n.-26-4448T=
NM_000930.4:c.-26-4448T=	NP_000921.1:n.-26-4448T=
NM_001319189.1:c.-26-4448T=	NP_001306118.1:n.-26-4448T=
NM_033011.3:c.-26-4448T=	NP_127509.1:n.-26-4448T=
NM_000930.5:c.-26-4448T= MANE Select	NP_000921.1:n.-26-4448T=
NM_001319189.2:c.-26-4448T=	NP_001306118.1:n.-26-4448T=
NM_033011.4:c.-26-4448T=	NP_127509.1:n.-26-4448T=