Canonical Allele Identifier: CA1302666469

Gene: TANK PSMD14-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.161236117T= , CM000664.2:g.161236117T=	GRCh38
NC_000002.11:g.162092628T= , CM000664.1:g.162092628T=	GRCh37
NC_000002.10:g.161800874T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392749.7:c.*599T= (TANK) MANE Select	ENSP00000376505.2:n.*599T=
ENST00000259075.6:c.*599T= (TANK)	ENSP00000259075.2:n.*599T=
ENST00000392749.6:c.*599T= (TANK)	ENSP00000376505.2:n.*599T=
ENST00000405852.5:c.*727T= (TANK)	ENSP00000385487.1:n.*727T=
ENST00000437623.1:c.1653T= (TANK)	ENSP00000412556.1:n.1653T=
NM_001199135.1:c.*599T= (TANK)	NP_001186064.1:n.*599T=
NM_004180.2:c.*599T= (TANK)	NP_004171.2:n.*599T=
NR_110593.1:n.348+12407A= (PSMD14-DT)
XM_005246207.3:c.*599T= (TANK)	XP_005246264.2:n.*599T=
XM_005246208.3:c.*599T= (TANK)	XP_005246265.1:n.*599T=
XM_005246210.2:c.*599T= (TANK)	XP_005246267.1:n.*599T=
XM_005246211.1:c.*599T= (TANK)	XP_005246268.1:n.*599T=
XM_011510455.1:c.*599T= (TANK)	XP_011508757.1:n.*599T=
NM_001199135.2:c.*599T= (TANK)	NP_001186064.1:n.*599T=
XM_017003093.1:c.*599T= (TANK)	XP_016858582.1:n.*599T=
XM_017003094.1:c.*599T= (TANK)	XP_016858583.1:n.*599T=
XM_017003095.1:c.*599T= (TANK)	XP_016858584.1:n.*599T=
XM_017003096.1:c.*599T= (TANK)	XP_016858585.1:n.*599T=
XM_017003097.1:c.*599T= (TANK)	XP_016858586.1:n.*599T=
XM_024452333.1:c.*599T= (TANK)	XP_024308101.1:n.*599T=
XM_024452335.1:c.*599T= (TANK)	XP_024308103.1:n.*599T=
XM_024452337.1:c.*599T= (TANK)	XP_024308105.1:n.*599T=
NM_001199135.3:c.*599T= (TANK) MANE Select	NP_001186064.1:n.*599T=
NM_004180.3:c.*599T= (TANK)	NP_004171.2:n.*599T=