Canonical Allele Identifier: CA2625288923

Gene: MAX

Linked Data

• gnomAD v4: 14-65075384-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075384A>G , CM000676.2:g.65075384A>G	GRCh38
NC_000014.8:g.65542102A>G , CM000676.1:g.65542102A>G	GRCh37
NC_000014.7:g.64611855A>G	NCBI36
NG_029830.1:g.32126T>C , LRG_530:g.32126T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000556979.6:c.*2028T>C	ENSP00000452378.1:n.*2028T>C
ENST00000358664.9:c.*1092T>C MANE Select	ENSP00000351490.4:n.*1092T>C
ENST00000651648.1:c.145-5015T>C	ENSP00000498863.1:n.145-5015T>C
ENST00000284165.10:c.*2419T>C	ENSP00000284165.6:n.*2419T>C
ENST00000341653.6:c.171+18324T>C	ENSP00000342482.2:n.171+18324T>C
ENST00000358402.8:c.*1092T>C	ENSP00000351175.4:n.*1092T>C
ENST00000394606.6:c.*1348T>C	ENSP00000378104.2:n.*1348T>C
ENST00000555932.5:c.*1067T>C	ENSP00000450763.1:n.*1067T>C
ENST00000618858.4:c.*1364T>C	ENSP00000480127.1:n.*1364T>C
NM_001271069.1:c.144+18324T>C	NP_001257998.1:n.144+18324T>C
NM_002382.4:c.*1092T>C	NP_002373.3:n.*1092T>C
NM_145112.2:c.*1092T>C	NP_660087.1:n.*1092T>C
NM_145113.2:c.*1364T>C	NP_660088.1:n.*1364T>C
NM_197957.3:c.171+18324T>C	NP_932061.1:n.171+18324T>C
NR_073137.1:n.1699T>C
XR_429315.2:n.1862T>C
NM_001320415.1:c.*1092T>C	NP_001307344.1:n.*1092T>C
XM_017021312.2:c.*1092T>C	XP_016876801.1:n.*1092T>C
XM_017021313.1:c.*1092T>C	XP_016876802.1:n.*1092T>C
XR_001750326.2:n.1920T>C
XR_001750327.2:n.1839T>C
XR_002957553.1:n.2353T>C
XR_943450.3:n.1943T>C
XR_943451.3:n.1959T>C
XR_943452.3:n.1904T>C
NM_001320415.2:c.*1092T>C	NP_001307344.1:n.*1092T>C
NM_002382.5:c.*1092T>C MANE Select	NP_002373.3:n.*1092T>C
NM_145112.3:c.*1092T>C	NP_660087.1:n.*1092T>C
NM_145113.3:c.*1364T>C	NP_660088.1:n.*1364T>C
NM_001271069.2:c.144+18324T>C	NP_001257998.1:n.144+18324T>C
NM_197957.4:c.171+18324T>C	NP_932061.1:n.171+18324T>C