Canonical Allele Identifier: CA2142951588

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076437_65076441delinsGAGAC , CM000676.2:g.65076437_65076441delinsGAGAC	GRCh38
NC_000014.8:g.65543155_65543159delinsGAGAC , CM000676.1:g.65543155_65543159delinsGAGAC	GRCh37
NC_000014.7:g.64612908_64612912delinsGAGAC	NCBI36
NG_029830.1:g.31069_31073delinsGTCTC , LRG_530:g.31069_31073delinsGTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*35_*39delinsGTCTC	ENSP00000452206.2:n.*35_*39delinsGTCTC
ENST00000556979.6:c.*971_*975delinsGTCTC	ENSP00000452378.1:n.*971_*975delinsGTCTC
ENST00000358664.9:c.*35_*39delinsGTCTC MANE Select	ENSP00000351490.4:n.*35_*39delinsGTCTC
ENST00000651648.1:c.145-6072_145-6068delinsGTCTC	ENSP00000498863.1:n.145-6072_145-6068delinsGTCTC
ENST00000284165.10:c.*1362_*1366delinsGTCTC	ENSP00000284165.6:n.*1362_*1366delinsGTCTC
ENST00000341653.6:c.171+17267_171+17271delinsGTCTC	ENSP00000342482.2:n.171+17267_171+17271delinsGTCTC
ENST00000358402.8:c.*35_*39delinsGTCTC	ENSP00000351175.4:n.*35_*39delinsGTCTC
ENST00000358664.8:c.*35_*39delinsGTCTC	ENSP00000351490.4:n.*35_*39delinsGTCTC
ENST00000394606.6:c.*291_*295delinsGTCTC	ENSP00000378104.2:n.*291_*295delinsGTCTC
ENST00000555419.5:c.410_414delinsGTCTC	ENSP00000452405.1:n.410_414delinsGTCTC
ENST00000555932.5:c.*10_*14delinsGTCTC	ENSP00000450763.1:n.*10_*14delinsGTCTC
ENST00000618858.4:c.*307_*311delinsGTCTC	ENSP00000480127.1:n.*307_*311delinsGTCTC
NM_001271069.1:c.144+17267_144+17271delinsGTCTC	NP_001257998.1:n.144+17267_144+17271delinsGTCTC
NM_002382.4:c.*35_*39delinsGTCTC	NP_002373.3:n.*35_*39delinsGTCTC
NM_145112.2:c.*35_*39delinsGTCTC	NP_660087.1:n.*35_*39delinsGTCTC
NM_145113.2:c.*307_*311delinsGTCTC	NP_660088.1:n.*307_*311delinsGTCTC
NM_197957.3:c.171+17267_171+17271delinsGTCTC	NP_932061.1:n.171+17267_171+17271delinsGTCTC
NR_073137.1:n.642_646delinsGTCTC
XR_429315.2:n.805_809delinsGTCTC
NM_001320415.1:c.*35_*39delinsGTCTC	NP_001307344.1:n.*35_*39delinsGTCTC
XM_017021312.2:c.*35_*39delinsGTCTC	XP_016876801.1:n.*35_*39delinsGTCTC
XM_017021313.1:c.*35_*39delinsGTCTC	XP_016876802.1:n.*35_*39delinsGTCTC
XR_001750326.2:n.863_867delinsGTCTC
XR_001750327.2:n.782_786delinsGTCTC
XR_002957553.1:n.1296_1300delinsGTCTC
XR_943450.3:n.886_890delinsGTCTC
XR_943451.3:n.902_906delinsGTCTC
XR_943452.3:n.847_851delinsGTCTC
NM_001320415.2:c.*35_*39delinsGTCTC	NP_001307344.1:n.*35_*39delinsGTCTC
NM_002382.5:c.*35_*39delinsGTCTC MANE Select	NP_002373.3:n.*35_*39delinsGTCTC
NM_145112.3:c.*35_*39delinsGTCTC	NP_660087.1:n.*35_*39delinsGTCTC
NM_145113.3:c.*307_*311delinsGTCTC	NP_660088.1:n.*307_*311delinsGTCTC
NM_001271069.2:c.144+17267_144+17271delinsGTCTC	NP_001257998.1:n.144+17267_144+17271delinsGTCTC
NM_197957.4:c.171+17267_171+17271delinsGTCTC	NP_932061.1:n.171+17267_171+17271delinsGTCTC