Canonical Allele Identifier: CA2142951337
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075907T= , CM000676.2:g.65075907T= GRCh38
NC_000014.8:g.65542625T= , CM000676.1:g.65542625T= GRCh37
NC_000014.7:g.64612378T= NCBI36
NG_029830.1:g.31603A= , LRG_530:g.31603A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*569A= ENSP00000452206.2:n.*569A=
ENST00000556979.6:c.*1505A= ENSP00000452378.1:n.*1505A=
ENST00000358664.9:c.*569A= MANE Select ENSP00000351490.4:n.*569A=
ENST00000651648.1:c.145-5538A= ENSP00000498863.1:n.145-5538A=
ENST00000284165.10:c.*1896A= ENSP00000284165.6:n.*1896A=
ENST00000341653.6:c.171+17801A= ENSP00000342482.2:n.171+17801A=
ENST00000358402.8:c.*569A= ENSP00000351175.4:n.*569A=
ENST00000358664.8:c.*569A= ENSP00000351490.4:n.*569A=
ENST00000394606.6:c.*825A= ENSP00000378104.2:n.*825A=
ENST00000555932.5:c.*544A= ENSP00000450763.1:n.*544A=
ENST00000618858.4:c.*841A= ENSP00000480127.1:n.*841A=
NM_001271069.1:c.144+17801A= NP_001257998.1:n.144+17801A=
NM_002382.4:c.*569A= NP_002373.3:n.*569A=
NM_145112.2:c.*569A= NP_660087.1:n.*569A=
NM_145113.2:c.*841A= NP_660088.1:n.*841A=
NM_197957.3:c.171+17801A= NP_932061.1:n.171+17801A=
NR_073137.1:n.1176A=
XR_429315.2:n.1339A=
NM_001320415.1:c.*569A= NP_001307344.1:n.*569A=
XM_017021312.2:c.*569A= XP_016876801.1:n.*569A=
XM_017021313.1:c.*569A= XP_016876802.1:n.*569A=
XR_001750326.2:n.1397A=
XR_001750327.2:n.1316A=
XR_002957553.1:n.1830A=
XR_943450.3:n.1420A=
XR_943451.3:n.1436A=
XR_943452.3:n.1381A=
NM_001320415.2:c.*569A= NP_001307344.1:n.*569A=
NM_002382.5:c.*569A= MANE Select NP_002373.3:n.*569A=
NM_145112.3:c.*569A= NP_660087.1:n.*569A=
NM_145113.3:c.*841A= NP_660088.1:n.*841A=
NM_001271069.2:c.144+17801A= NP_001257998.1:n.144+17801A=
NM_197957.4:c.171+17801A= NP_932061.1:n.171+17801A=