Canonical Allele Identifier: CA2142952262
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65077991A= , CM000676.2:g.65077991A= GRCh38
NC_000014.8:g.65544709A= , CM000676.1:g.65544709A= GRCh37
NC_000014.7:g.64614462A= NCBI36
NG_029830.1:g.29519T= , LRG_530:g.29519T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.-3T= ENSP00000452206.2:n.-3T=
ENST00000556979.6:c.217T= ENSP00000452378.1:p.Tyr73=
ENST00000358664.9:c.217T= MANE Select ENSP00000351490.4:p.Tyr73=
ENST00000651648.1:c.145-7622T= ENSP00000498863.1:n.145-7622T=
ENST00000284165.10:c.217T= ENSP00000284165.6:p.Tyr73=
ENST00000341653.6:c.171+15717T= ENSP00000342482.2:n.171+15717T=
ENST00000358402.8:c.190T= ENSP00000351175.4:p.Tyr64=
ENST00000358664.8:c.217T= ENSP00000351490.4:p.Tyr73=
ENST00000394606.6:c.217T= ENSP00000378104.2:p.Tyr73=
ENST00000553928.5:c.217T= ENSP00000451907.1:p.Tyr73=
ENST00000553951.1:n.294T=
ENST00000555419.5:c.109T= ENSP00000452405.1:p.Tyr37=
ENST00000555667.5:c.190T= ENSP00000452286.1:p.Tyr64=
ENST00000555932.5:c.37-1328T= ENSP00000450763.1:n.37-1328T=
ENST00000556443.5:c.190T= ENSP00000450818.1:p.Tyr64=
ENST00000556892.5:c.-3T= ENSP00000452206.1:n.-3T=
ENST00000556979.5:c.217T= ENSP00000452378.1:p.Tyr73=
ENST00000557277.5:c.-58T= ENSP00000450955.1:n.-58T=
ENST00000557746.5:c.190T= ENSP00000452197.1:p.Tyr64=
ENST00000618858.4:c.217T= ENSP00000480127.1:p.Tyr73=
NM_001271069.1:c.144+15717T= NP_001257998.1:n.144+15717T=
NM_002382.4:c.217T= NP_002373.3:p.Tyr73=
NM_145112.2:c.190T= NP_660087.1:p.Tyr64=
NM_145113.2:c.217T= NP_660088.1:p.Tyr73=
NM_197957.3:c.171+15717T= NP_932061.1:n.171+15717T=
NR_073137.1:n.341T=
XM_011536773.1:c.217T= XP_011535075.1:p.Tyr73=
XR_429315.2:n.419T=
XR_943450.1:n.419T=
XR_943451.1:n.419T=
XR_943452.1:n.381T=
NM_001320415.1:c.-58T= NP_001307344.1:n.-58T=
XM_011536773.3:c.217T= XP_011535075.1:p.Tyr73=
XM_017021312.2:c.-58T= XP_016876801.1:n.-58T=
XM_017021313.1:c.-58T= XP_016876802.1:n.-58T=
XR_001750326.2:n.380T=
XR_001750327.2:n.380T=
XR_002957553.1:n.410T=
XR_943450.3:n.419T=
XR_943451.3:n.419T=
XR_943452.3:n.380T=
NM_001320415.2:c.-58T= NP_001307344.1:n.-58T=
NM_002382.5:c.217T= MANE Select NP_002373.3:p.Tyr73=
NM_145112.3:c.190T= NP_660087.1:p.Tyr64=
NM_145113.3:c.217T= NP_660088.1:p.Tyr73=
NM_001271069.2:c.144+15717T= NP_001257998.1:n.144+15717T=
NM_197957.4:c.171+15717T= NP_932061.1:n.171+15717T=