Canonical Allele Identifier: CA2142951260
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075745_65075766delinsGCTTCACTGCTGCCATCTCCCA , CM000676.2:g.65075745_65075766delinsGCTTCACTGCTGCCATCTCCCA GRCh38
NC_000014.8:g.65542463_65542484delinsGCTTCACTGCTGCCATCTCCCA , CM000676.1:g.65542463_65542484delinsGCTTCACTGCTGCCATCTCCCA GRCh37
NC_000014.7:g.64612216_64612237delinsGCTTCACTGCTGCCATCTCCCA NCBI36
NG_029830.1:g.31744_31765delinsTGGGAGATGGCAGCAGTGAAGC , LRG_530:g.31744_31765delinsTGGGAGATGGCAGCAGTGAAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000452206.2:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
ENST00000556979.6:c.*1646_*1667delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000452378.1:n.*1646_*1667delinsTGGGAGATGGCAGCAGTGAAGC
ENST00000358664.9:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC MANE Select ENSP00000351490.4:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
ENST00000651648.1:c.145-5397_145-5376delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000498863.1:n.145-5397_145-5376delinsTGGGAGATGGCAGCAGTG...
ENST00000284165.10:c.*2037_*2058delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000284165.6:n.*2037_*2058delinsTGGGAGATGGCAGCAGTGAAGC
ENST00000341653.6:c.171+17942_171+17963delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000342482.2:n.171+17942_171+17963delinsTGGGAGATGGCAGCAG...
ENST00000358402.8:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000351175.4:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
ENST00000358664.8:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000351490.4:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
ENST00000394606.6:c.*966_*987delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000378104.2:n.*966_*987delinsTGGGAGATGGCAGCAGTGAAGC
ENST00000555932.5:c.*685_*706delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000450763.1:n.*685_*706delinsTGGGAGATGGCAGCAGTGAAGC
ENST00000618858.4:c.*982_*1003delinsTGGGAGATGGCAGCAGTGAAGC ENSP00000480127.1:n.*982_*1003delinsTGGGAGATGGCAGCAGTGAAGC
NM_001271069.1:c.144+17942_144+17963delinsTGGGAGATGGCAGCAGTGAAGC NP_001257998.1:n.144+17942_144+17963delinsTGGGAGATGGCAGCAGTGA...
NM_002382.4:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC NP_002373.3:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
NM_145112.2:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC NP_660087.1:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
NM_145113.2:c.*982_*1003delinsTGGGAGATGGCAGCAGTGAAGC NP_660088.1:n.*982_*1003delinsTGGGAGATGGCAGCAGTGAAGC
NM_197957.3:c.171+17942_171+17963delinsTGGGAGATGGCAGCAGTGAAGC NP_932061.1:n.171+17942_171+17963delinsTGGGAGATGGCAGCAGTGAAGC...
NR_073137.1:n.1317_1338delinsTGGGAGATGGCAGCAGTGAAGC
XR_429315.2:n.1480_1501delinsTGGGAGATGGCAGCAGTGAAGC
NM_001320415.1:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC NP_001307344.1:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
XM_017021312.2:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC XP_016876801.1:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
XM_017021313.1:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC XP_016876802.1:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
XR_001750326.2:n.1538_1559delinsTGGGAGATGGCAGCAGTGAAGC
XR_001750327.2:n.1457_1478delinsTGGGAGATGGCAGCAGTGAAGC
XR_002957553.1:n.1971_1992delinsTGGGAGATGGCAGCAGTGAAGC
XR_943450.3:n.1561_1582delinsTGGGAGATGGCAGCAGTGAAGC
XR_943451.3:n.1577_1598delinsTGGGAGATGGCAGCAGTGAAGC
XR_943452.3:n.1522_1543delinsTGGGAGATGGCAGCAGTGAAGC
NM_001320415.2:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC NP_001307344.1:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
NM_002382.5:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC MANE Select NP_002373.3:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
NM_145112.3:c.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC NP_660087.1:n.*710_*731delinsTGGGAGATGGCAGCAGTGAAGC
NM_145113.3:c.*982_*1003delinsTGGGAGATGGCAGCAGTGAAGC NP_660088.1:n.*982_*1003delinsTGGGAGATGGCAGCAGTGAAGC
NM_001271069.2:c.144+17942_144+17963delinsTGGGAGATGGCAGCAGTGAAGC NP_001257998.1:n.144+17942_144+17963delinsTGGGAGATGGCAGCAGTGA...
NM_197957.4:c.171+17942_171+17963delinsTGGGAGATGGCAGCAGTGAAGC NP_932061.1:n.171+17942_171+17963delinsTGGGAGATGGCAGCAGTGAAGC...