Canonical Allele Identifier: CA11130712
Gene: TANK HGNC NCBI

Linked Data

dbSNP Id: rs10930013

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.161213814G>A , CM000664.2:g.161213814G>A GRCh38
NC_000002.11:g.162070325G>A , CM000664.1:g.162070325G>A GRCh37
NC_000002.10:g.161778571G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392749.7:c.327+9021G>A MANE Select ENSP00000376505.2:n.327+9021G>A
ENST00000259075.6:c.327+9021G>A ENSP00000259075.2:n.327+9021G>A
ENST00000392749.6:c.327+9021G>A ENSP00000376505.2:n.327+9021G>A
ENST00000402568.5:c.504+9021G>A ENSP00000384235.1:n.504+9021G>A
ENST00000405852.5:c.327+9021G>A ENSP00000385487.1:n.327+9021G>A
ENST00000406287.5:c.501+9021G>A ENSP00000384492.1:n.501+9021G>A
ENST00000429217.5:c.330+9021G>A ENSP00000411041.1:n.330+9021G>A
ENST00000432002.5:c.330+9021G>A ENSP00000398157.1:n.330+9021G>A
ENST00000432692.6:c.328-2575G>A ENSP00000412622.1:n.328-2575G>A
ENST00000456358.5:c.405+9021G>A ENSP00000392776.1:n.405+9021G>A
ENST00000457887.5:c.328-5910G>A ENSP00000388930.1:n.328-5910G>A
ENST00000468831.5:n.507+9021G>A
NM_001199135.1:c.327+9021G>A NP_001186064.1:n.327+9021G>A
NM_004180.2:c.327+9021G>A NP_004171.2:n.327+9021G>A
XM_005246207.3:c.405+9021G>A XP_005246264.2:n.405+9021G>A
XM_005246208.3:c.504+9021G>A XP_005246265.1:n.504+9021G>A
XM_005246210.2:c.330+9021G>A XP_005246267.1:n.330+9021G>A
XM_005246211.1:c.330+9021G>A XP_005246268.1:n.330+9021G>A
XM_011510455.1:c.330+9021G>A XP_011508757.1:n.330+9021G>A
NM_001199135.2:c.327+9021G>A NP_001186064.1:n.327+9021G>A
XM_017003093.1:c.501+9021G>A XP_016858582.1:n.501+9021G>A
XM_017003094.1:c.468+9021G>A XP_016858583.1:n.468+9021G>A
XM_017003095.1:c.396+9021G>A XP_016858584.1:n.396+9021G>A
XM_017003096.1:c.327+9021G>A XP_016858585.1:n.327+9021G>A
XM_017003097.1:c.327+9021G>A XP_016858586.1:n.327+9021G>A
XM_024452333.1:c.501+9021G>A XP_024308101.1:n.501+9021G>A
XM_024452335.1:c.414+9021G>A XP_024308103.1:n.414+9021G>A
XM_024452337.1:c.-133+9021G>A XP_024308105.1:n.-133+9021G>A
NM_001199135.3:c.327+9021G>A MANE Select NP_001186064.1:n.327+9021G>A
NM_004180.3:c.327+9021G>A NP_004171.2:n.327+9021G>A