Canonical Allele Identifier: CA2142951323
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075874A= , CM000676.2:g.65075874A= GRCh38
NC_000014.8:g.65542592A= , CM000676.1:g.65542592A= GRCh37
NC_000014.7:g.64612345A= NCBI36
NG_029830.1:g.31636T= , LRG_530:g.31636T=

Transcript Alleles

HGVS Amino-acid change
ENST00000556892.6:c.*602T= ENSP00000452206.2:n.*602T=
ENST00000556979.6:c.*1538T= ENSP00000452378.1:n.*1538T=
ENST00000358664.9:c.*602T= MANE Select ENSP00000351490.4:n.*602T=
ENST00000651648.1:c.145-5505T= ENSP00000498863.1:n.145-5505T=
ENST00000284165.10:c.*1929T= ENSP00000284165.6:n.*1929T=
ENST00000341653.6:c.171+17834T= ENSP00000342482.2:n.171+17834T=
ENST00000358402.8:c.*602T= ENSP00000351175.4:n.*602T=
ENST00000358664.8:c.*602T= ENSP00000351490.4:n.*602T=
ENST00000394606.6:c.*858T= ENSP00000378104.2:n.*858T=
ENST00000555932.5:c.*577T= ENSP00000450763.1:n.*577T=
ENST00000618858.4:c.*874T= ENSP00000480127.1:n.*874T=
NM_001271069.1:c.144+17834T= NP_001257998.1:n.144+17834T=
NM_002382.4:c.*602T= NP_002373.3:n.*602T=
NM_145112.2:c.*602T= NP_660087.1:n.*602T=
NM_145113.2:c.*874T= NP_660088.1:n.*874T=
NM_197957.3:c.171+17834T= NP_932061.1:n.171+17834T=
NR_073137.1:n.1209T=
XR_429315.2:n.1372T=
NM_001320415.1:c.*602T= NP_001307344.1:n.*602T=
XM_017021312.2:c.*602T= XP_016876801.1:n.*602T=
XM_017021313.1:c.*602T= XP_016876802.1:n.*602T=
XR_001750326.2:n.1430T=
XR_001750327.2:n.1349T=
XR_002957553.1:n.1863T=
XR_943450.3:n.1453T=
XR_943451.3:n.1469T=
XR_943452.3:n.1414T=
NM_001320415.2:c.*602T= NP_001307344.1:n.*602T=
NM_002382.5:c.*602T= MANE Select NP_002373.3:n.*602T=
NM_145112.3:c.*602T= NP_660087.1:n.*602T=
NM_145113.3:c.*874T= NP_660088.1:n.*874T=
NM_001271069.2:c.144+17834T= NP_001257998.1:n.144+17834T=
NM_197957.4:c.171+17834T= NP_932061.1:n.171+17834T=