Canonical Allele Identifier: CA2142951620

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076520C= , CM000676.2:g.65076520C=	GRCh38
NC_000014.8:g.65543238C= , CM000676.1:g.65543238C=	GRCh37
NC_000014.7:g.64612991C=	NCBI36
NG_029830.1:g.30990G= , LRG_530:g.30990G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.220G=	ENSP00000452206.2:p.Glu74=
ENST00000556979.6:c.*892G=	ENSP00000452378.1:n.*892G=
ENST00000358664.9:c.439G= MANE Select	ENSP00000351490.4:p.Glu147=
ENST00000651648.1:c.145-6151G=	ENSP00000498863.1:n.145-6151G=
ENST00000284165.10:c.*1283G=	ENSP00000284165.6:n.*1283G=
ENST00000341653.6:c.171+17188G=	ENSP00000342482.2:n.171+17188G=
ENST00000358402.8:c.412G=	ENSP00000351175.4:p.Glu138=
ENST00000358664.8:c.439G=	ENSP00000351490.4:p.Glu147=
ENST00000394606.6:c.*212G=	ENSP00000378104.2:n.*212G=
ENST00000553928.5:c.*228G=	ENSP00000451907.1:n.*228G=
ENST00000555419.5:c.331G=	ENSP00000452405.1:p.Glu111=
ENST00000555932.5:c.180G=	ENSP00000450763.1:p.Leu60=
ENST00000557277.5:c.250G=	ENSP00000450955.1:p.Glu84=
ENST00000618858.4:c.*228G=	ENSP00000480127.1:n.*228G=
NM_001271069.1:c.144+17188G=	NP_001257998.1:n.144+17188G=
NM_002382.4:c.439G=	NP_002373.3:p.Glu147=
NM_145112.2:c.412G=	NP_660087.1:p.Glu138=
NM_145113.2:c.*228G=	NP_660088.1:n.*228G=
NM_197957.3:c.171+17188G=	NP_932061.1:n.171+17188G=
NR_073137.1:n.563G=
XR_429315.2:n.726G=
NM_001320415.1:c.250G=	NP_001307344.1:p.Glu84=
XM_017021312.2:c.250G=	XP_016876801.1:p.Glu84=
XM_017021313.1:c.250G=	XP_016876802.1:p.Glu84=
XR_001750326.2:n.784G=
XR_001750327.2:n.703G=
XR_002957553.1:n.1217G=
XR_943450.3:n.807G=
XR_943451.3:n.823G=
XR_943452.3:n.768G=
NM_001320415.2:c.250G=	NP_001307344.1:p.Glu84=
NM_002382.5:c.439G= MANE Select	NP_002373.3:p.Glu147=
NM_145112.3:c.412G=	NP_660087.1:p.Glu138=
NM_145113.3:c.*228G=	NP_660088.1:n.*228G=
NM_001271069.2:c.144+17188G=	NP_001257998.1:n.144+17188G=
NM_197957.4:c.171+17188G=	NP_932061.1:n.171+17188G=