Canonical Allele Identifier: CA2625289523

Gene: MAX

Linked Data

• gnomAD v4: 14-65076093-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076093A>C , CM000676.2:g.65076093A>C	GRCh38
NC_000014.8:g.65542811A>C , CM000676.1:g.65542811A>C	GRCh37
NC_000014.7:g.64612564A>C	NCBI36
NG_029830.1:g.31417T>G , LRG_530:g.31417T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*383T>G	ENSP00000452206.2:n.*383T>G
ENST00000556979.6:c.*1319T>G	ENSP00000452378.1:n.*1319T>G
ENST00000358664.9:c.*383T>G MANE Select	ENSP00000351490.4:n.*383T>G
ENST00000651648.1:c.145-5724T>G	ENSP00000498863.1:n.145-5724T>G
ENST00000284165.10:c.*1710T>G	ENSP00000284165.6:n.*1710T>G
ENST00000341653.6:c.171+17615T>G	ENSP00000342482.2:n.171+17615T>G
ENST00000358402.8:c.*383T>G	ENSP00000351175.4:n.*383T>G
ENST00000358664.8:c.*383T>G	ENSP00000351490.4:n.*383T>G
ENST00000394606.6:c.*639T>G	ENSP00000378104.2:n.*639T>G
ENST00000555419.5:c.758T>G	ENSP00000452405.1:n.758T>G
ENST00000555932.5:c.*358T>G	ENSP00000450763.1:n.*358T>G
ENST00000618858.4:c.*655T>G	ENSP00000480127.1:n.*655T>G
NM_001271069.1:c.144+17615T>G	NP_001257998.1:n.144+17615T>G
NM_002382.4:c.*383T>G	NP_002373.3:n.*383T>G
NM_145112.2:c.*383T>G	NP_660087.1:n.*383T>G
NM_145113.2:c.*655T>G	NP_660088.1:n.*655T>G
NM_197957.3:c.171+17615T>G	NP_932061.1:n.171+17615T>G
NR_073137.1:n.990T>G
XR_429315.2:n.1153T>G
NM_001320415.1:c.*383T>G	NP_001307344.1:n.*383T>G
XM_017021312.2:c.*383T>G	XP_016876801.1:n.*383T>G
XM_017021313.1:c.*383T>G	XP_016876802.1:n.*383T>G
XR_001750326.2:n.1211T>G
XR_001750327.2:n.1130T>G
XR_002957553.1:n.1644T>G
XR_943450.3:n.1234T>G
XR_943451.3:n.1250T>G
XR_943452.3:n.1195T>G
NM_001320415.2:c.*383T>G	NP_001307344.1:n.*383T>G
NM_002382.5:c.*383T>G MANE Select	NP_002373.3:n.*383T>G
NM_145112.3:c.*383T>G	NP_660087.1:n.*383T>G
NM_145113.3:c.*655T>G	NP_660088.1:n.*655T>G
NM_001271069.2:c.144+17615T>G	NP_001257998.1:n.144+17615T>G
NM_197957.4:c.171+17615T>G	NP_932061.1:n.171+17615T>G