Canonical Allele Identifier: CA2661654356

Gene: TANK PSMD14-DT

Linked Data

• gnomAD v4: 2-161236040-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.161236040A>T , CM000664.2:g.161236040A>T	GRCh38
NC_000002.11:g.162092551A>T , CM000664.1:g.162092551A>T	GRCh37
NC_000002.10:g.161800797A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392749.7:c.*522A>T (TANK) MANE Select	ENSP00000376505.2:n.*522A>T
ENST00000259075.6:c.*522A>T (TANK)	ENSP00000259075.2:n.*522A>T
ENST00000392749.6:c.*522A>T (TANK)	ENSP00000376505.2:n.*522A>T
ENST00000405852.5:c.*650A>T (TANK)	ENSP00000385487.1:n.*650A>T
ENST00000437623.1:c.1576A>T (TANK)	ENSP00000412556.1:n.1576A>T
NM_001199135.1:c.*522A>T (TANK)	NP_001186064.1:n.*522A>T
NM_004180.2:c.*522A>T (TANK)	NP_004171.2:n.*522A>T
NR_110593.1:n.348+12484T>A (PSMD14-DT)
XM_005246207.3:c.*522A>T (TANK)	XP_005246264.2:n.*522A>T
XM_005246208.3:c.*522A>T (TANK)	XP_005246265.1:n.*522A>T
XM_005246210.2:c.*522A>T (TANK)	XP_005246267.1:n.*522A>T
XM_005246211.1:c.*522A>T (TANK)	XP_005246268.1:n.*522A>T
XM_011510455.1:c.*522A>T (TANK)	XP_011508757.1:n.*522A>T
NM_001199135.2:c.*522A>T (TANK)	NP_001186064.1:n.*522A>T
XM_017003093.1:c.*522A>T (TANK)	XP_016858582.1:n.*522A>T
XM_017003094.1:c.*522A>T (TANK)	XP_016858583.1:n.*522A>T
XM_017003095.1:c.*522A>T (TANK)	XP_016858584.1:n.*522A>T
XM_017003096.1:c.*522A>T (TANK)	XP_016858585.1:n.*522A>T
XM_017003097.1:c.*522A>T (TANK)	XP_016858586.1:n.*522A>T
XM_024452333.1:c.*522A>T (TANK)	XP_024308101.1:n.*522A>T
XM_024452335.1:c.*522A>T (TANK)	XP_024308103.1:n.*522A>T
XM_024452337.1:c.*522A>T (TANK)	XP_024308105.1:n.*522A>T
NM_001199135.3:c.*522A>T (TANK) MANE Select	NP_001186064.1:n.*522A>T
NM_004180.3:c.*522A>T (TANK)	NP_004171.2:n.*522A>T