Canonical Allele Identifier: CA2142951649
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65076582G= , CM000676.2:g.65076582G= GRCh38
NC_000014.8:g.65543300G= , CM000676.1:g.65543300G= GRCh37
NC_000014.7:g.64613053G= NCBI36
NG_029830.1:g.30928C= , LRG_530:g.30928C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.158C= ENSP00000452206.2:p.Ala53=
ENST00000556979.6:c.*830C= ENSP00000452378.1:n.*830C=
ENST00000358664.9:c.377C= MANE Select ENSP00000351490.4:p.Ala126=
ENST00000651648.1:c.145-6213C= ENSP00000498863.1:n.145-6213C=
ENST00000284165.10:c.*1221C= ENSP00000284165.6:n.*1221C=
ENST00000341653.6:c.171+17126C= ENSP00000342482.2:n.171+17126C=
ENST00000358402.8:c.350C= ENSP00000351175.4:p.Ala117=
ENST00000358664.8:c.377C= ENSP00000351490.4:p.Ala126=
ENST00000394606.6:c.*150C= ENSP00000378104.2:n.*150C=
ENST00000553928.5:c.*166C= ENSP00000451907.1:n.*166C=
ENST00000555419.5:c.269C= ENSP00000452405.1:p.Ala90=
ENST00000555932.5:c.118C= ENSP00000450763.1:p.Pro40=
ENST00000557277.5:c.188C= ENSP00000450955.1:p.Ala63=
ENST00000618858.4:c.*166C= ENSP00000480127.1:n.*166C=
NM_001271069.1:c.144+17126C= NP_001257998.1:n.144+17126C=
NM_002382.4:c.377C= NP_002373.3:p.Ala126=
NM_145112.2:c.350C= NP_660087.1:p.Ala117=
NM_145113.2:c.*166C= NP_660088.1:n.*166C=
NM_197957.3:c.171+17126C= NP_932061.1:n.171+17126C=
NR_073137.1:n.501C=
XR_429315.2:n.664C=
XR_943450.1:n.745C=
XR_943451.1:n.761C=
XR_943452.1:n.707C=
NM_001320415.1:c.188C= NP_001307344.1:p.Ala63=
XM_017021312.2:c.188C= XP_016876801.1:p.Ala63=
XM_017021313.1:c.188C= XP_016876802.1:p.Ala63=
XR_001750326.2:n.722C=
XR_001750327.2:n.641C=
XR_002957553.1:n.1155C=
XR_943450.3:n.745C=
XR_943451.3:n.761C=
XR_943452.3:n.706C=
NM_001320415.2:c.188C= NP_001307344.1:p.Ala63=
NM_002382.5:c.377C= MANE Select NP_002373.3:p.Ala126=
NM_145112.3:c.350C= NP_660087.1:p.Ala117=
NM_145113.3:c.*166C= NP_660088.1:n.*166C=
NM_001271069.2:c.144+17126C= NP_001257998.1:n.144+17126C=
NM_197957.4:c.171+17126C= NP_932061.1:n.171+17126C=