Canonical Allele Identifier: CA2801908526

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076466C>A , CM000676.2:g.65076466C>A	GRCh38
NC_000014.8:g.65543184C>A , CM000676.1:g.65543184C>A	GRCh37
NC_000014.7:g.64612937C>A	NCBI36
NG_029830.1:g.31044G>T , LRG_530:g.31044G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*10G>T	ENSP00000452206.2:n.*10G>T
ENST00000556979.6:c.*946G>T	ENSP00000452378.1:n.*946G>T
ENST00000358664.9:c.*10G>T MANE Select	ENSP00000351490.4:n.*10G>T
ENST00000651648.1:c.145-6097G>T	ENSP00000498863.1:n.145-6097G>T
ENST00000284165.10:c.*1337G>T	ENSP00000284165.6:n.*1337G>T
ENST00000341653.6:c.171+17242G>T	ENSP00000342482.2:n.171+17242G>T
ENST00000358402.8:c.*10G>T	ENSP00000351175.4:n.*10G>T
ENST00000358664.8:c.*10G>T	ENSP00000351490.4:n.*10G>T
ENST00000394606.6:c.*266G>T	ENSP00000378104.2:n.*266G>T
ENST00000553928.5:c.*282G>T	ENSP00000451907.1:n.*282G>T
ENST00000555419.5:c.385G>T	ENSP00000452405.1:n.385G>T
ENST00000555932.5:c.234G>T	ENSP00000450763.1:p.Gly78=
ENST00000557277.5:c.*10G>T	ENSP00000450955.1:n.*10G>T
ENST00000618858.4:c.*282G>T	ENSP00000480127.1:n.*282G>T
NM_001271069.1:c.144+17242G>T	NP_001257998.1:n.144+17242G>T
NM_002382.4:c.*10G>T	NP_002373.3:n.*10G>T
NM_145112.2:c.*10G>T	NP_660087.1:n.*10G>T
NM_145113.2:c.*282G>T	NP_660088.1:n.*282G>T
NM_197957.3:c.171+17242G>T	NP_932061.1:n.171+17242G>T
NR_073137.1:n.617G>T
XR_429315.2:n.780G>T
NM_001320415.1:c.*10G>T	NP_001307344.1:n.*10G>T
XM_017021312.2:c.*10G>T	XP_016876801.1:n.*10G>T
XM_017021313.1:c.*10G>T	XP_016876802.1:n.*10G>T
XR_001750326.2:n.838G>T
XR_001750327.2:n.757G>T
XR_002957553.1:n.1271G>T
XR_943450.3:n.861G>T
XR_943451.3:n.877G>T
XR_943452.3:n.822G>T
NM_001320415.2:c.*10G>T	NP_001307344.1:n.*10G>T
NM_002382.5:c.*10G>T MANE Select	NP_002373.3:n.*10G>T
NM_145112.3:c.*10G>T	NP_660087.1:n.*10G>T
NM_145113.3:c.*282G>T	NP_660088.1:n.*282G>T
NM_001271069.2:c.144+17242G>T	NP_001257998.1:n.144+17242G>T
NM_197957.4:c.171+17242G>T	NP_932061.1:n.171+17242G>T