Canonical Allele Identifier: CA2625288880

Gene: MAX

Linked Data

• gnomAD v4: 14-65075327-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075327A>C , CM000676.2:g.65075327A>C	GRCh38
NC_000014.8:g.65542045A>C , CM000676.1:g.65542045A>C	GRCh37
NC_000014.7:g.64611798A>C	NCBI36
NG_029830.1:g.32183T>G , LRG_530:g.32183T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2085T>G	ENSP00000452378.1:n.*2085T>G
ENST00000358664.9:c.*1149T>G MANE Select	ENSP00000351490.4:n.*1149T>G
ENST00000651648.1:c.145-4958T>G	ENSP00000498863.1:n.145-4958T>G
ENST00000284165.10:c.*2476T>G	ENSP00000284165.6:n.*2476T>G
ENST00000341653.6:c.171+18381T>G	ENSP00000342482.2:n.171+18381T>G
ENST00000358402.8:c.*1149T>G	ENSP00000351175.4:n.*1149T>G
ENST00000394606.6:c.*1405T>G	ENSP00000378104.2:n.*1405T>G
ENST00000555932.5:c.*1124T>G	ENSP00000450763.1:n.*1124T>G
ENST00000618858.4:c.*1421T>G	ENSP00000480127.1:n.*1421T>G
NM_001271069.1:c.144+18381T>G	NP_001257998.1:n.144+18381T>G
NM_002382.4:c.*1149T>G	NP_002373.3:n.*1149T>G
NM_145112.2:c.*1149T>G	NP_660087.1:n.*1149T>G
NM_145113.2:c.*1421T>G	NP_660088.1:n.*1421T>G
NM_197957.3:c.171+18381T>G	NP_932061.1:n.171+18381T>G
NR_073137.1:n.1756T>G
XR_429315.2:n.1919T>G
NM_001320415.1:c.*1149T>G	NP_001307344.1:n.*1149T>G
XM_017021312.2:c.*1149T>G	XP_016876801.1:n.*1149T>G
XM_017021313.1:c.*1149T>G	XP_016876802.1:n.*1149T>G
XR_001750326.2:n.1977T>G
XR_001750327.2:n.1896T>G
XR_002957553.1:n.2410T>G
XR_943450.3:n.2000T>G
XR_943451.3:n.2016T>G
XR_943452.3:n.1961T>G
NM_001320415.2:c.*1149T>G	NP_001307344.1:n.*1149T>G
NM_002382.5:c.*1149T>G MANE Select	NP_002373.3:n.*1149T>G
NM_145112.3:c.*1149T>G	NP_660087.1:n.*1149T>G
NM_145113.3:c.*1421T>G	NP_660088.1:n.*1421T>G
NM_001271069.2:c.144+18381T>G	NP_001257998.1:n.144+18381T>G
NM_197957.4:c.171+18381T>G	NP_932061.1:n.171+18381T>G