Canonical Allele Identifier: CA2142970905

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65102448C= , CM000676.2:g.65102448C=	GRCh38
NC_000014.8:g.65569166C= , CM000676.1:g.65569166C=	GRCh37
NC_000014.7:g.64638919C=	NCBI36
NG_029830.1:g.5062G= , LRG_530:g.5062G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.-157+61G=	ENSP00000452206.2:n.-157+61G=
ENST00000556979.6:c.-109G=	ENSP00000452378.1:n.-109G=
ENST00000358664.9:c.-109G= MANE Select	ENSP00000351490.4:n.-109G=
ENST00000246163.2:c.-109G=	ENSP00000246163.2:n.-109G=
ENST00000284165.10:c.-109G=	ENSP00000284165.6:n.-109G=
ENST00000358402.8:c.-109G=	ENSP00000351175.4:n.-109G=
ENST00000358664.8:c.-109G=	ENSP00000351490.4:n.-109G=
ENST00000394606.6:c.-109G=	ENSP00000378104.2:n.-109G=
ENST00000554709.1:n.70G=
ENST00000555667.5:c.-109G=	ENSP00000452286.1:n.-109G=
ENST00000555932.5:c.-109G=	ENSP00000450763.1:n.-109G=
ENST00000556443.5:c.-109G=	ENSP00000450818.1:n.-109G=
ENST00000556702.1:n.31G=
ENST00000556892.5:c.-157+61G=	ENSP00000452206.1:n.-157+61G=
ENST00000556979.5:c.-109G=	ENSP00000452378.1:n.-109G=
ENST00000557277.5:c.-239+61G=	ENSP00000450955.1:n.-239+61G=
ENST00000557746.5:c.-109G=	ENSP00000452197.1:n.-109G=
ENST00000618858.4:c.-109G=	ENSP00000480127.1:n.-109G=
NM_001271068.1:c.-109G=	NP_001257997.1:n.-109G=
NM_001271069.1:c.-109G=	NP_001257998.1:n.-109G=
NM_002382.4:c.-109G=	NP_002373.3:n.-109G=
NM_145112.2:c.-109G=	NP_660087.1:n.-109G=
NM_145113.2:c.-109G=	NP_660088.1:n.-109G=
NM_145114.2:c.-109G=	NP_660089.1:n.-109G=
NM_197957.3:c.-109G=	NP_932061.1:n.-109G=
NR_073137.1:n.187+61G=
NR_073138.1:n.187+61G=
XM_011536773.1:c.-109G=	XP_011535075.1:n.-109G=
XR_429315.2:n.94G=
XR_943450.1:n.94G=
XR_943451.1:n.94G=
XR_943452.1:n.83G=
NM_001320415.1:c.-383G=	NP_001307344.1:n.-383G=
XM_011536773.3:c.-109G=	XP_011535075.1:n.-109G=
XM_017021312.2:c.-356G=	XP_016876801.1:n.-356G=
XR_001750326.2:n.82G=
XR_001750327.2:n.82G=
XR_002957553.1:n.85G=
XR_943450.3:n.94G=
XR_943451.3:n.94G=
XR_943452.3:n.82G=
NM_001320415.2:c.-383G=	NP_001307344.1:n.-383G=
NM_002382.5:c.-109G= MANE Select	NP_002373.3:n.-109G=
NM_145112.3:c.-109G=	NP_660087.1:n.-109G=
NM_145113.3:c.-109G=	NP_660088.1:n.-109G=
NM_001271068.2:c.-109G=	NP_001257997.1:n.-109G=
NM_001271069.2:c.-109G=	NP_001257998.1:n.-109G=
NM_145114.3:c.-109G=	NP_660089.1:n.-109G=
NM_197957.4:c.-109G=	NP_932061.1:n.-109G=