Canonical Allele Identifier: CA2142951641

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076562C= , CM000676.2:g.65076562C=	GRCh38
NC_000014.8:g.65543280C= , CM000676.1:g.65543280C=	GRCh37
NC_000014.7:g.64613033C=	NCBI36
NG_029830.1:g.30948G= , LRG_530:g.30948G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.178G=	ENSP00000452206.2:p.Ala60=
ENST00000556979.6:c.*850G=	ENSP00000452378.1:n.*850G=
ENST00000358664.9:c.397G= MANE Select	ENSP00000351490.4:p.Ala133=
ENST00000651648.1:c.145-6193G=	ENSP00000498863.1:n.145-6193G=
ENST00000284165.10:c.*1241G=	ENSP00000284165.6:n.*1241G=
ENST00000341653.6:c.171+17146G=	ENSP00000342482.2:n.171+17146G=
ENST00000358402.8:c.370G=	ENSP00000351175.4:p.Ala124=
ENST00000358664.8:c.397G=	ENSP00000351490.4:p.Ala133=
ENST00000394606.6:c.*170G=	ENSP00000378104.2:n.*170G=
ENST00000553928.5:c.*186G=	ENSP00000451907.1:n.*186G=
ENST00000555419.5:c.289G=	ENSP00000452405.1:p.Ala97=
ENST00000555932.5:c.138G=	ENSP00000450763.1:p.Leu46=
ENST00000557277.5:c.208G=	ENSP00000450955.1:p.Ala70=
ENST00000618858.4:c.*186G=	ENSP00000480127.1:n.*186G=
NM_001271069.1:c.144+17146G=	NP_001257998.1:n.144+17146G=
NM_002382.4:c.397G=	NP_002373.3:p.Ala133=
NM_145112.2:c.370G=	NP_660087.1:p.Ala124=
NM_145113.2:c.*186G=	NP_660088.1:n.*186G=
NM_197957.3:c.171+17146G=	NP_932061.1:n.171+17146G=
NR_073137.1:n.521G=
XR_429315.2:n.684G=
NM_001320415.1:c.208G=	NP_001307344.1:p.Ala70=
XM_017021312.2:c.208G=	XP_016876801.1:p.Ala70=
XM_017021313.1:c.208G=	XP_016876802.1:p.Ala70=
XR_001750326.2:n.742G=
XR_001750327.2:n.661G=
XR_002957553.1:n.1175G=
XR_943450.3:n.765G=
XR_943451.3:n.781G=
XR_943452.3:n.726G=
NM_001320415.2:c.208G=	NP_001307344.1:p.Ala70=
NM_002382.5:c.397G= MANE Select	NP_002373.3:p.Ala133=
NM_145112.3:c.370G=	NP_660087.1:p.Ala124=
NM_145113.3:c.*186G=	NP_660088.1:n.*186G=
NM_001271069.2:c.144+17146G=	NP_001257998.1:n.144+17146G=
NM_197957.4:c.171+17146G=	NP_932061.1:n.171+17146G=