Canonical Allele Identifier: CA2801908485

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075355C>A , CM000676.2:g.65075355C>A	GRCh38
NC_000014.8:g.65542073C>A , CM000676.1:g.65542073C>A	GRCh37
NC_000014.7:g.64611826C>A	NCBI36
NG_029830.1:g.32155G>T , LRG_530:g.32155G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2057G>T	ENSP00000452378.1:n.*2057G>T
ENST00000358664.9:c.*1121G>T MANE Select	ENSP00000351490.4:n.*1121G>T
ENST00000651648.1:c.145-4986G>T	ENSP00000498863.1:n.145-4986G>T
ENST00000284165.10:c.*2448G>T	ENSP00000284165.6:n.*2448G>T
ENST00000341653.6:c.171+18353G>T	ENSP00000342482.2:n.171+18353G>T
ENST00000358402.8:c.*1121G>T	ENSP00000351175.4:n.*1121G>T
ENST00000394606.6:c.*1377G>T	ENSP00000378104.2:n.*1377G>T
ENST00000555932.5:c.*1096G>T	ENSP00000450763.1:n.*1096G>T
ENST00000618858.4:c.*1393G>T	ENSP00000480127.1:n.*1393G>T
NM_001271069.1:c.144+18353G>T	NP_001257998.1:n.144+18353G>T
NM_002382.4:c.*1121G>T	NP_002373.3:n.*1121G>T
NM_145112.2:c.*1121G>T	NP_660087.1:n.*1121G>T
NM_145113.2:c.*1393G>T	NP_660088.1:n.*1393G>T
NM_197957.3:c.171+18353G>T	NP_932061.1:n.171+18353G>T
NR_073137.1:n.1728G>T
XR_429315.2:n.1891G>T
NM_001320415.1:c.*1121G>T	NP_001307344.1:n.*1121G>T
XM_017021312.2:c.*1121G>T	XP_016876801.1:n.*1121G>T
XM_017021313.1:c.*1121G>T	XP_016876802.1:n.*1121G>T
XR_001750326.2:n.1949G>T
XR_001750327.2:n.1868G>T
XR_002957553.1:n.2382G>T
XR_943450.3:n.1972G>T
XR_943451.3:n.1988G>T
XR_943452.3:n.1933G>T
NM_001320415.2:c.*1121G>T	NP_001307344.1:n.*1121G>T
NM_002382.5:c.*1121G>T MANE Select	NP_002373.3:n.*1121G>T
NM_145112.3:c.*1121G>T	NP_660087.1:n.*1121G>T
NM_145113.3:c.*1393G>T	NP_660088.1:n.*1393G>T
NM_001271069.2:c.144+18353G>T	NP_001257998.1:n.144+18353G>T
NM_197957.4:c.171+18353G>T	NP_932061.1:n.171+18353G>T