Canonical Allele Identifier: CA2625288930
Gene: MAX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075396_65075397insCTGTC , CM000676.2:g.65075396_65075397insCTGTC GRCh38
NC_000014.8:g.65542114_65542115insCTGTC , CM000676.1:g.65542114_65542115insCTGTC GRCh37
NC_000014.7:g.64611867_64611868insCTGTC NCBI36
NG_029830.1:g.32114_32115insACAGG , LRG_530:g.32114_32115insACAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000556979.6:c.*2016_*2017insACAGG ENSP00000452378.1:n.*2016_*2017insACAGG
ENST00000358664.9:c.*1080_*1081insACAGG MANE Select ENSP00000351490.4:n.*1080_*1081insACAGG
ENST00000651648.1:c.145-5027_145-5026insACAGG ENSP00000498863.1:n.145-5027_145-5026insACAGG
ENST00000284165.10:c.*2407_*2408insACAGG ENSP00000284165.6:n.*2407_*2408insACAGG
ENST00000341653.6:c.171+18312_171+18313insACAGG ENSP00000342482.2:n.171+18312_171+18313insACAGG
ENST00000358402.8:c.*1080_*1081insACAGG ENSP00000351175.4:n.*1080_*1081insACAGG
ENST00000394606.6:c.*1336_*1337insACAGG ENSP00000378104.2:n.*1336_*1337insACAGG
ENST00000555932.5:c.*1055_*1056insACAGG ENSP00000450763.1:n.*1055_*1056insACAGG
ENST00000618858.4:c.*1352_*1353insACAGG ENSP00000480127.1:n.*1352_*1353insACAGG
NM_001271069.1:c.144+18312_144+18313insACAGG NP_001257998.1:n.144+18312_144+18313insACAGG
NM_002382.4:c.*1080_*1081insACAGG NP_002373.3:n.*1080_*1081insACAGG
NM_145112.2:c.*1080_*1081insACAGG NP_660087.1:n.*1080_*1081insACAGG
NM_145113.2:c.*1352_*1353insACAGG NP_660088.1:n.*1352_*1353insACAGG
NM_197957.3:c.171+18312_171+18313insACAGG NP_932061.1:n.171+18312_171+18313insACAGG
NR_073137.1:n.1687_1688insACAGG
XR_429315.2:n.1850_1851insACAGG
NM_001320415.1:c.*1080_*1081insACAGG NP_001307344.1:n.*1080_*1081insACAGG
XM_017021312.2:c.*1080_*1081insACAGG XP_016876801.1:n.*1080_*1081insACAGG
XM_017021313.1:c.*1080_*1081insACAGG XP_016876802.1:n.*1080_*1081insACAGG
XR_001750326.2:n.1908_1909insACAGG
XR_001750327.2:n.1827_1828insACAGG
XR_002957553.1:n.2341_2342insACAGG
XR_943450.3:n.1931_1932insACAGG
XR_943451.3:n.1947_1948insACAGG
XR_943452.3:n.1892_1893insACAGG
NM_001320415.2:c.*1080_*1081insACAGG NP_001307344.1:n.*1080_*1081insACAGG
NM_002382.5:c.*1080_*1081insACAGG MANE Select NP_002373.3:n.*1080_*1081insACAGG
NM_145112.3:c.*1080_*1081insACAGG NP_660087.1:n.*1080_*1081insACAGG
NM_145113.3:c.*1352_*1353insACAGG NP_660088.1:n.*1352_*1353insACAGG
NM_001271069.2:c.144+18312_144+18313insACAGG NP_001257998.1:n.144+18312_144+18313insACAGG
NM_197957.4:c.171+18312_171+18313insACAGG NP_932061.1:n.171+18312_171+18313insACAGG