Canonical Allele Identifier: CA2142952254
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65077979_65077980delinsTC , CM000676.2:g.65077979_65077980delinsTC GRCh38
NC_000014.8:g.65544697_65544698delinsTC , CM000676.1:g.65544697_65544698delinsTC GRCh37
NC_000014.7:g.64614450_64614451delinsTC NCBI36
NG_029830.1:g.29530_29531delinsGA , LRG_530:g.29530_29531delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.9_10delinsGA ENSP00000452206.2:p.Arg3=
ENST00000556979.6:c.228_229delinsGA ENSP00000452378.1:p.Arg76=
ENST00000358664.9:c.228_229delinsGA MANE Select ENSP00000351490.4:p.Arg76=
ENST00000651648.1:c.145-7611_145-7610delinsGA ENSP00000498863.1:n.145-7611_145-7610delinsGA
ENST00000284165.10:c.228_229delinsGA ENSP00000284165.6:p.Arg76=
ENST00000341653.6:c.171+15728_171+15729delinsGA ENSP00000342482.2:n.171+15728_171+15729delinsGA
ENST00000358402.8:c.201_202delinsGA ENSP00000351175.4:p.Arg67=
ENST00000358664.8:c.228_229delinsGA ENSP00000351490.4:p.Arg76=
ENST00000394606.6:c.228_229delinsGA ENSP00000378104.2:p.Arg76=
ENST00000553928.5:c.228_229delinsGA ENSP00000451907.1:p.Arg76=
ENST00000553951.1:n.305_306delinsGA
ENST00000555419.5:c.120_121delinsGA ENSP00000452405.1:p.Arg40=
ENST00000555667.5:c.201_202delinsGA ENSP00000452286.1:p.Arg67=
ENST00000555932.5:c.37-1317_37-1316delinsGA ENSP00000450763.1:n.37-1317_37-1316delinsGA
ENST00000556443.5:c.201_202delinsGA ENSP00000450818.1:p.Arg67=
ENST00000556892.5:c.9_10delinsGA ENSP00000452206.1:p.Arg3=
ENST00000556979.5:c.228_229delinsGA ENSP00000452378.1:p.Arg76=
ENST00000557277.5:c.-47_-46delinsGA ENSP00000450955.1:n.-47_-46delinsGA
ENST00000557746.5:c.201_202delinsGA ENSP00000452197.1:p.Arg67=
ENST00000618858.4:c.228_229delinsGA ENSP00000480127.1:p.Arg76=
NM_001271069.1:c.144+15728_144+15729delinsGA NP_001257998.1:n.144+15728_144+15729delinsGA
NM_002382.4:c.228_229delinsGA NP_002373.3:p.Arg76=
NM_145112.2:c.201_202delinsGA NP_660087.1:p.Arg67=
NM_145113.2:c.228_229delinsGA NP_660088.1:p.Arg76=
NM_197957.3:c.171+15728_171+15729delinsGA NP_932061.1:n.171+15728_171+15729delinsGA
NR_073137.1:n.352_353delinsGA
XM_011536773.1:c.228_229delinsGA XP_011535075.1:p.Arg76=
XR_429315.2:n.430_431delinsGA
XR_943450.1:n.430_431delinsGA
XR_943451.1:n.430_431delinsGA
XR_943452.1:n.392_393delinsGA
NM_001320415.1:c.-47_-46delinsGA NP_001307344.1:n.-47_-46delinsGA
XM_011536773.3:c.228_229delinsGA XP_011535075.1:p.Arg76=
XM_017021312.2:c.-47_-46delinsGA XP_016876801.1:n.-47_-46delinsGA
XM_017021313.1:c.-47_-46delinsGA XP_016876802.1:n.-47_-46delinsGA
XR_001750326.2:n.391_392delinsGA
XR_001750327.2:n.391_392delinsGA
XR_002957553.1:n.421_422delinsGA
XR_943450.3:n.430_431delinsGA
XR_943451.3:n.430_431delinsGA
XR_943452.3:n.391_392delinsGA
NM_001320415.2:c.-47_-46delinsGA NP_001307344.1:n.-47_-46delinsGA
NM_002382.5:c.228_229delinsGA MANE Select NP_002373.3:p.Arg76=
NM_145112.3:c.201_202delinsGA NP_660087.1:p.Arg67=
NM_145113.3:c.228_229delinsGA NP_660088.1:p.Arg76=
NM_001271069.2:c.144+15728_144+15729delinsGA NP_001257998.1:n.144+15728_144+15729delinsGA
NM_197957.4:c.171+15728_171+15729delinsGA NP_932061.1:n.171+15728_171+15729delinsGA