Canonical Allele Identifier: CA2142952385

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65078252A= , CM000676.2:g.65078252A=	GRCh38
NC_000014.8:g.65544970A= , CM000676.1:g.65544970A=	GRCh37
NC_000014.7:g.64614723A=	NCBI36
NG_029830.1:g.29258T= , LRG_530:g.29258T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.-48-216T=	ENSP00000452206.2:n.-48-216T=
ENST00000556979.6:c.172-216T=	ENSP00000452378.1:n.172-216T=
ENST00000358664.9:c.172-216T= MANE Select	ENSP00000351490.4:n.172-216T=
ENST00000651648.1:c.145-7883T=	ENSP00000498863.1:n.145-7883T=
ENST00000284165.10:c.172-216T=	ENSP00000284165.6:n.172-216T=
ENST00000341653.6:c.171+15456T=	ENSP00000342482.2:n.171+15456T=
ENST00000358402.8:c.145-216T=	ENSP00000351175.4:n.145-216T=
ENST00000358664.8:c.172-216T=	ENSP00000351490.4:n.172-216T=
ENST00000394606.6:c.172-216T=	ENSP00000378104.2:n.172-216T=
ENST00000553928.5:c.172-216T=	ENSP00000451907.1:n.172-216T=
ENST00000553951.1:n.249-216T=
ENST00000555419.5:c.64-216T=	ENSP00000452405.1:n.64-216T=
ENST00000555667.5:c.145-216T=	ENSP00000452286.1:n.145-216T=
ENST00000555932.5:c.37-1589T=	ENSP00000450763.1:n.37-1589T=
ENST00000556443.5:c.145-216T=	ENSP00000450818.1:n.145-216T=
ENST00000556892.5:c.-48-216T=	ENSP00000452206.1:n.-48-216T=
ENST00000556979.5:c.172-216T=	ENSP00000452378.1:n.172-216T=
ENST00000557277.5:c.-103-216T=	ENSP00000450955.1:n.-103-216T=
ENST00000557746.5:c.145-216T=	ENSP00000452197.1:n.145-216T=
ENST00000618858.4:c.172-216T=	ENSP00000480127.1:n.172-216T=
NM_001271069.1:c.144+15456T=	NP_001257998.1:n.144+15456T=
NM_002382.4:c.172-216T=	NP_002373.3:n.172-216T=
NM_145112.2:c.145-216T=	NP_660087.1:n.145-216T=
NM_145113.2:c.172-216T=	NP_660088.1:n.172-216T=
NM_197957.3:c.171+15456T=	NP_932061.1:n.171+15456T=
NR_073137.1:n.296-216T=
XM_011536773.1:c.172-216T=	XP_011535075.1:n.172-216T=
XR_429315.2:n.374-216T=
XR_943450.1:n.374-216T=
XR_943451.1:n.374-216T=
XR_943452.1:n.336-216T=
NM_001320415.1:c.-103-216T=	NP_001307344.1:n.-103-216T=
XM_011536773.3:c.172-216T=	XP_011535075.1:n.172-216T=
XM_017021312.2:c.-103-216T=	XP_016876801.1:n.-103-216T=
XM_017021313.1:c.-103-216T=	XP_016876802.1:n.-103-216T=
XR_001750326.2:n.335-216T=
XR_001750327.2:n.335-216T=
XR_002957553.1:n.365-216T=
XR_943450.3:n.374-216T=
XR_943451.3:n.374-216T=
XR_943452.3:n.335-216T=
NM_001320415.2:c.-103-216T=	NP_001307344.1:n.-103-216T=
NM_002382.5:c.172-216T= MANE Select	NP_002373.3:n.172-216T=
NM_145112.3:c.145-216T=	NP_660087.1:n.145-216T=
NM_145113.3:c.172-216T=	NP_660088.1:n.172-216T=
NM_001271069.2:c.144+15456T=	NP_001257998.1:n.144+15456T=
NM_197957.4:c.171+15456T=	NP_932061.1:n.171+15456T=