Canonical Allele Identifier: CA2575554365

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075598G>C , CM000676.2:g.65075598G>C	GRCh38
NC_000014.8:g.65542316G>C , CM000676.1:g.65542316G>C	GRCh37
NC_000014.7:g.64612069G>C	NCBI36
NG_029830.1:g.31912C>G , LRG_530:g.31912C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*878C>G	ENSP00000452206.2:n.*878C>G
ENST00000556979.6:c.*1814C>G	ENSP00000452378.1:n.*1814C>G
ENST00000358664.9:c.*878C>G MANE Select	ENSP00000351490.4:n.*878C>G
ENST00000651648.1:c.145-5229C>G	ENSP00000498863.1:n.145-5229C>G
ENST00000284165.10:c.*2205C>G	ENSP00000284165.6:n.*2205C>G
ENST00000341653.6:c.171+18110C>G	ENSP00000342482.2:n.171+18110C>G
ENST00000358402.8:c.*878C>G	ENSP00000351175.4:n.*878C>G
ENST00000358664.8:c.*878C>G	ENSP00000351490.4:n.*878C>G
ENST00000394606.6:c.*1134C>G	ENSP00000378104.2:n.*1134C>G
ENST00000555932.5:c.*853C>G	ENSP00000450763.1:n.*853C>G
ENST00000618858.4:c.*1150C>G	ENSP00000480127.1:n.*1150C>G
NM_001271069.1:c.144+18110C>G	NP_001257998.1:n.144+18110C>G
NM_002382.4:c.*878C>G	NP_002373.3:n.*878C>G
NM_145112.2:c.*878C>G	NP_660087.1:n.*878C>G
NM_145113.2:c.*1150C>G	NP_660088.1:n.*1150C>G
NM_197957.3:c.171+18110C>G	NP_932061.1:n.171+18110C>G
NR_073137.1:n.1485C>G
XR_429315.2:n.1648C>G
NM_001320415.1:c.*878C>G	NP_001307344.1:n.*878C>G
XM_017021312.2:c.*878C>G	XP_016876801.1:n.*878C>G
XM_017021313.1:c.*878C>G	XP_016876802.1:n.*878C>G
XR_001750326.2:n.1706C>G
XR_001750327.2:n.1625C>G
XR_002957553.1:n.2139C>G
XR_943450.3:n.1729C>G
XR_943451.3:n.1745C>G
XR_943452.3:n.1690C>G
NM_001320415.2:c.*878C>G	NP_001307344.1:n.*878C>G
NM_002382.5:c.*878C>G MANE Select	NP_002373.3:n.*878C>G
NM_145112.3:c.*878C>G	NP_660087.1:n.*878C>G
NM_145113.3:c.*1150C>G	NP_660088.1:n.*1150C>G
NM_001271069.2:c.144+18110C>G	NP_001257998.1:n.144+18110C>G
NM_197957.4:c.171+18110C>G	NP_932061.1:n.171+18110C>G