Canonical Allele Identifier: CA2142951082
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075365C= , CM000676.2:g.65075365C= GRCh38
NC_000014.8:g.65542083C= , CM000676.1:g.65542083C= GRCh37
NC_000014.7:g.64611836C= NCBI36
NG_029830.1:g.32145G= , LRG_530:g.32145G=

Transcript Alleles

HGVS Amino-acid change
ENST00000556979.6:c.*2047G= ENSP00000452378.1:n.*2047G=
ENST00000358664.9:c.*1111G= MANE Select ENSP00000351490.4:n.*1111G=
ENST00000651648.1:c.145-4996G= ENSP00000498863.1:n.145-4996G=
ENST00000284165.10:c.*2438G= ENSP00000284165.6:n.*2438G=
ENST00000341653.6:c.171+18343G= ENSP00000342482.2:n.171+18343G=
ENST00000358402.8:c.*1111G= ENSP00000351175.4:n.*1111G=
ENST00000394606.6:c.*1367G= ENSP00000378104.2:n.*1367G=
ENST00000555932.5:c.*1086G= ENSP00000450763.1:n.*1086G=
ENST00000618858.4:c.*1383G= ENSP00000480127.1:n.*1383G=
NM_001271069.1:c.144+18343G= NP_001257998.1:n.144+18343G=
NM_002382.4:c.*1111G= NP_002373.3:n.*1111G=
NM_145112.2:c.*1111G= NP_660087.1:n.*1111G=
NM_145113.2:c.*1383G= NP_660088.1:n.*1383G=
NM_197957.3:c.171+18343G= NP_932061.1:n.171+18343G=
NR_073137.1:n.1718G=
XR_429315.2:n.1881G=
NM_001320415.1:c.*1111G= NP_001307344.1:n.*1111G=
XM_017021312.2:c.*1111G= XP_016876801.1:n.*1111G=
XM_017021313.1:c.*1111G= XP_016876802.1:n.*1111G=
XR_001750326.2:n.1939G=
XR_001750327.2:n.1858G=
XR_002957553.1:n.2372G=
XR_943450.3:n.1962G=
XR_943451.3:n.1978G=
XR_943452.3:n.1923G=
NM_001320415.2:c.*1111G= NP_001307344.1:n.*1111G=
NM_002382.5:c.*1111G= MANE Select NP_002373.3:n.*1111G=
NM_145112.3:c.*1111G= NP_660087.1:n.*1111G=
NM_145113.3:c.*1383G= NP_660088.1:n.*1383G=
NM_001271069.2:c.144+18343G= NP_001257998.1:n.144+18343G=
NM_197957.4:c.171+18343G= NP_932061.1:n.171+18343G=