Canonical Allele Identifier: CA2625289496

Gene: MAX

Linked Data

• gnomAD v4: 14-65076076-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076076C>A , CM000676.2:g.65076076C>A	GRCh38
NC_000014.8:g.65542794C>A , CM000676.1:g.65542794C>A	GRCh37
NC_000014.7:g.64612547C>A	NCBI36
NG_029830.1:g.31434G>T , LRG_530:g.31434G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*400G>T	ENSP00000452206.2:n.*400G>T
ENST00000556979.6:c.*1336G>T	ENSP00000452378.1:n.*1336G>T
ENST00000358664.9:c.*400G>T MANE Select	ENSP00000351490.4:n.*400G>T
ENST00000651648.1:c.145-5707G>T	ENSP00000498863.1:n.145-5707G>T
ENST00000284165.10:c.*1727G>T	ENSP00000284165.6:n.*1727G>T
ENST00000341653.6:c.171+17632G>T	ENSP00000342482.2:n.171+17632G>T
ENST00000358402.8:c.*400G>T	ENSP00000351175.4:n.*400G>T
ENST00000358664.8:c.*400G>T	ENSP00000351490.4:n.*400G>T
ENST00000394606.6:c.*656G>T	ENSP00000378104.2:n.*656G>T
ENST00000555932.5:c.*375G>T	ENSP00000450763.1:n.*375G>T
ENST00000618858.4:c.*672G>T	ENSP00000480127.1:n.*672G>T
NM_001271069.1:c.144+17632G>T	NP_001257998.1:n.144+17632G>T
NM_002382.4:c.*400G>T	NP_002373.3:n.*400G>T
NM_145112.2:c.*400G>T	NP_660087.1:n.*400G>T
NM_145113.2:c.*672G>T	NP_660088.1:n.*672G>T
NM_197957.3:c.171+17632G>T	NP_932061.1:n.171+17632G>T
NR_073137.1:n.1007G>T
XR_429315.2:n.1170G>T
NM_001320415.1:c.*400G>T	NP_001307344.1:n.*400G>T
XM_017021312.2:c.*400G>T	XP_016876801.1:n.*400G>T
XM_017021313.1:c.*400G>T	XP_016876802.1:n.*400G>T
XR_001750326.2:n.1228G>T
XR_001750327.2:n.1147G>T
XR_002957553.1:n.1661G>T
XR_943450.3:n.1251G>T
XR_943451.3:n.1267G>T
XR_943452.3:n.1212G>T
NM_001320415.2:c.*400G>T	NP_001307344.1:n.*400G>T
NM_002382.5:c.*400G>T MANE Select	NP_002373.3:n.*400G>T
NM_145112.3:c.*400G>T	NP_660087.1:n.*400G>T
NM_145113.3:c.*672G>T	NP_660088.1:n.*672G>T
NM_001271069.2:c.144+17632G>T	NP_001257998.1:n.144+17632G>T
NM_197957.4:c.171+17632G>T	NP_932061.1:n.171+17632G>T