Canonical Allele Identifier: CA2556612548

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075387C>T , CM000676.2:g.65075387C>T	GRCh38
NC_000014.8:g.65542105C>T , CM000676.1:g.65542105C>T	GRCh37
NC_000014.7:g.64611858C>T	NCBI36
NG_029830.1:g.32123G>A , LRG_530:g.32123G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000556979.6:c.*2025G>A	ENSP00000452378.1:n.*2025G>A
ENST00000358664.9:c.*1089G>A MANE Select	ENSP00000351490.4:n.*1089G>A
ENST00000651648.1:c.145-5018G>A	ENSP00000498863.1:n.145-5018G>A
ENST00000284165.10:c.*2416G>A	ENSP00000284165.6:n.*2416G>A
ENST00000341653.6:c.171+18321G>A	ENSP00000342482.2:n.171+18321G>A
ENST00000358402.8:c.*1089G>A	ENSP00000351175.4:n.*1089G>A
ENST00000394606.6:c.*1345G>A	ENSP00000378104.2:n.*1345G>A
ENST00000555932.5:c.*1064G>A	ENSP00000450763.1:n.*1064G>A
ENST00000618858.4:c.*1361G>A	ENSP00000480127.1:n.*1361G>A
NM_001271069.1:c.144+18321G>A	NP_001257998.1:n.144+18321G>A
NM_002382.4:c.*1089G>A	NP_002373.3:n.*1089G>A
NM_145112.2:c.*1089G>A	NP_660087.1:n.*1089G>A
NM_145113.2:c.*1361G>A	NP_660088.1:n.*1361G>A
NM_197957.3:c.171+18321G>A	NP_932061.1:n.171+18321G>A
NR_073137.1:n.1696G>A
XR_429315.2:n.1859G>A
NM_001320415.1:c.*1089G>A	NP_001307344.1:n.*1089G>A
XM_017021312.2:c.*1089G>A	XP_016876801.1:n.*1089G>A
XM_017021313.1:c.*1089G>A	XP_016876802.1:n.*1089G>A
XR_001750326.2:n.1917G>A
XR_001750327.2:n.1836G>A
XR_002957553.1:n.2350G>A
XR_943450.3:n.1940G>A
XR_943451.3:n.1956G>A
XR_943452.3:n.1901G>A
NM_001320415.2:c.*1089G>A	NP_001307344.1:n.*1089G>A
NM_002382.5:c.*1089G>A MANE Select	NP_002373.3:n.*1089G>A
NM_145112.3:c.*1089G>A	NP_660087.1:n.*1089G>A
NM_145113.3:c.*1361G>A	NP_660088.1:n.*1361G>A
NM_001271069.2:c.144+18321G>A	NP_001257998.1:n.144+18321G>A
NM_197957.4:c.171+18321G>A	NP_932061.1:n.171+18321G>A