Canonical Allele Identifier: CA195070

Gene: MAX

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65093706A>T , CM000676.2:g.65093706A>T	GRCh38
NC_000014.8:g.65560424A>T , CM000676.1:g.65560424A>T	GRCh37
NC_000014.7:g.64630177A>T	NCBI36
NG_029830.1:g.13804T>A , LRG_530:g.13804T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.-49+2T>A	ENSP00000452206.2:n.-49+2T>A
ENST00000556979.6:c.171+2T>A	ENSP00000452378.1:n.171+2T>A
ENST00000358664.9:c.171+2T>A MANE Select	ENSP00000351490.4:n.171+2T>A
ENST00000651648.1:c.144+2T>A	ENSP00000498863.1:n.144+2T>A
ENST00000246163.2:c.171+2T>A	ENSP00000246163.2:n.171+2T>A
ENST00000284165.10:c.171+2T>A	ENSP00000284165.6:n.171+2T>A
ENST00000341653.6:c.171+2T>A	ENSP00000342482.2:n.171+2T>A
ENST00000358402.8:c.144+2T>A	ENSP00000351175.4:n.144+2T>A
ENST00000358664.8:c.171+2T>A	ENSP00000351490.4:n.171+2T>A
ENST00000394606.6:c.171+2T>A	ENSP00000378104.2:n.171+2T>A
ENST00000553928.5:c.171+2T>A	ENSP00000451907.1:n.171+2T>A
ENST00000553951.1:n.248+2T>A
ENST00000554709.1:n.324T>A
ENST00000555419.5:c.63+7840T>A	ENSP00000452405.1:n.63+7840T>A
ENST00000555667.5:c.144+2T>A	ENSP00000452286.1:n.144+2T>A
ENST00000555932.5:c.36+8598T>A	ENSP00000450763.1:n.36+8598T>A
ENST00000556443.5:c.144+2T>A	ENSP00000450818.1:n.144+2T>A
ENST00000556702.1:n.312T>A
ENST00000556892.5:c.-49+2T>A	ENSP00000452206.1:n.-49+2T>A
ENST00000556979.5:c.171+2T>A	ENSP00000452378.1:n.171+2T>A
ENST00000557277.5:c.-104+2T>A	ENSP00000450955.1:n.-104+2T>A
ENST00000557746.5:c.144+2T>A	ENSP00000452197.1:n.144+2T>A
ENST00000618858.4:c.171+2T>A	ENSP00000480127.1:n.171+2T>A
NM_001271068.1:c.144+2T>A	NP_001257997.1:n.144+2T>A
NM_001271069.1:c.144+2T>A	NP_001257998.1:n.144+2T>A
NM_002382.4:c.171+2T>A	NP_002373.3:n.171+2T>A
NM_145112.2:c.144+2T>A	NP_660087.1:n.144+2T>A
NM_145113.2:c.171+2T>A	NP_660088.1:n.171+2T>A
NM_145114.2:c.171+2T>A	NP_660089.1:n.171+2T>A
NM_197957.3:c.171+2T>A	NP_932061.1:n.171+2T>A
NR_045122.1:n.290A>T
NR_073137.1:n.295+2T>A
NR_073138.1:n.295+2T>A
XM_011536773.1:c.171+2T>A	XP_011535075.1:n.171+2T>A
XR_429315.2:n.373+2T>A
XR_943450.1:n.373+2T>A
XR_943451.1:n.373+2T>A
XR_943452.1:n.335+2T>A
NM_001320415.1:c.-104+2T>A	NP_001307344.1:n.-104+2T>A
XM_011536773.3:c.171+2T>A	XP_011535075.1:n.171+2T>A
XM_017021312.2:c.-104+2T>A	XP_016876801.1:n.-104+2T>A
XM_017021313.1:c.-104+2T>A	XP_016876802.1:n.-104+2T>A
XR_001750326.2:n.334+2T>A
XR_001750327.2:n.334+2T>A
XR_002957553.1:n.364+2T>A
XR_943450.3:n.373+2T>A
XR_943451.3:n.373+2T>A
XR_943452.3:n.334+2T>A
NM_001320415.2:c.-104+2T>A	NP_001307344.1:n.-104+2T>A
NM_002382.5:c.171+2T>A MANE Select	NP_002373.3:n.171+2T>A
NM_145112.3:c.144+2T>A	NP_660087.1:n.144+2T>A
NM_145113.3:c.171+2T>A	NP_660088.1:n.171+2T>A
NM_001271068.2:c.144+2T>A	NP_001257997.1:n.144+2T>A
NM_001271069.2:c.144+2T>A	NP_001257998.1:n.144+2T>A
NM_145114.3:c.171+2T>A	NP_660089.1:n.171+2T>A
NM_197957.4:c.171+2T>A	NP_932061.1:n.171+2T>A