Canonical Allele Identifier: CA2142952363
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65078202_65078203delinsTA , CM000676.2:g.65078202_65078203delinsTA GRCh38
NC_000014.8:g.65544920_65544921delinsTA , CM000676.1:g.65544920_65544921delinsTA GRCh37
NC_000014.7:g.64614673_64614674delinsTA NCBI36
NG_029830.1:g.29307_29308delinsTA , LRG_530:g.29307_29308delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000556892.6:c.-48-167_-48-166delinsTA ENSP00000452206.2:n.-48-167_-48-166delinsTA
ENST00000556979.6:c.172-167_172-166delinsTA ENSP00000452378.1:n.172-167_172-166delinsTA
ENST00000358664.9:c.172-167_172-166delinsTA MANE Select ENSP00000351490.4:n.172-167_172-166delinsTA
ENST00000651648.1:c.145-7834_145-7833delinsTA ENSP00000498863.1:n.145-7834_145-7833delinsTA
ENST00000284165.10:c.172-167_172-166delinsTA ENSP00000284165.6:n.172-167_172-166delinsTA
ENST00000341653.6:c.171+15505_171+15506delinsTA ENSP00000342482.2:n.171+15505_171+15506delinsTA
ENST00000358402.8:c.145-167_145-166delinsTA ENSP00000351175.4:n.145-167_145-166delinsTA
ENST00000358664.8:c.172-167_172-166delinsTA ENSP00000351490.4:n.172-167_172-166delinsTA
ENST00000394606.6:c.172-167_172-166delinsTA ENSP00000378104.2:n.172-167_172-166delinsTA
ENST00000553928.5:c.172-167_172-166delinsTA ENSP00000451907.1:n.172-167_172-166delinsTA
ENST00000553951.1:n.249-167_249-166delinsTA
ENST00000555419.5:c.64-167_64-166delinsTA ENSP00000452405.1:n.64-167_64-166delinsTA
ENST00000555667.5:c.145-167_145-166delinsTA ENSP00000452286.1:n.145-167_145-166delinsTA
ENST00000555932.5:c.37-1540_37-1539delinsTA ENSP00000450763.1:n.37-1540_37-1539delinsTA
ENST00000556443.5:c.145-167_145-166delinsTA ENSP00000450818.1:n.145-167_145-166delinsTA
ENST00000556892.5:c.-48-167_-48-166delinsTA ENSP00000452206.1:n.-48-167_-48-166delinsTA
ENST00000556979.5:c.172-167_172-166delinsTA ENSP00000452378.1:n.172-167_172-166delinsTA
ENST00000557277.5:c.-103-167_-103-166delinsTA ENSP00000450955.1:n.-103-167_-103-166delinsTA
ENST00000557746.5:c.145-167_145-166delinsTA ENSP00000452197.1:n.145-167_145-166delinsTA
ENST00000618858.4:c.172-167_172-166delinsTA ENSP00000480127.1:n.172-167_172-166delinsTA
NM_001271069.1:c.144+15505_144+15506delinsTA NP_001257998.1:n.144+15505_144+15506delinsTA
NM_002382.4:c.172-167_172-166delinsTA NP_002373.3:n.172-167_172-166delinsTA
NM_145112.2:c.145-167_145-166delinsTA NP_660087.1:n.145-167_145-166delinsTA
NM_145113.2:c.172-167_172-166delinsTA NP_660088.1:n.172-167_172-166delinsTA
NM_197957.3:c.171+15505_171+15506delinsTA NP_932061.1:n.171+15505_171+15506delinsTA
NR_073137.1:n.296-167_296-166delinsTA
XM_011536773.1:c.172-167_172-166delinsTA XP_011535075.1:n.172-167_172-166delinsTA
XR_429315.2:n.374-167_374-166delinsTA
XR_943450.1:n.374-167_374-166delinsTA
XR_943451.1:n.374-167_374-166delinsTA
XR_943452.1:n.336-167_336-166delinsTA
NM_001320415.1:c.-103-167_-103-166delinsTA NP_001307344.1:n.-103-167_-103-166delinsTA
XM_011536773.3:c.172-167_172-166delinsTA XP_011535075.1:n.172-167_172-166delinsTA
XM_017021312.2:c.-103-167_-103-166delinsTA XP_016876801.1:n.-103-167_-103-166delinsTA
XM_017021313.1:c.-103-167_-103-166delinsTA XP_016876802.1:n.-103-167_-103-166delinsTA
XR_001750326.2:n.335-167_335-166delinsTA
XR_001750327.2:n.335-167_335-166delinsTA
XR_002957553.1:n.365-167_365-166delinsTA
XR_943450.3:n.374-167_374-166delinsTA
XR_943451.3:n.374-167_374-166delinsTA
XR_943452.3:n.335-167_335-166delinsTA
NM_001320415.2:c.-103-167_-103-166delinsTA NP_001307344.1:n.-103-167_-103-166delinsTA
NM_002382.5:c.172-167_172-166delinsTA MANE Select NP_002373.3:n.172-167_172-166delinsTA
NM_145112.3:c.145-167_145-166delinsTA NP_660087.1:n.145-167_145-166delinsTA
NM_145113.3:c.172-167_172-166delinsTA NP_660088.1:n.172-167_172-166delinsTA
NM_001271069.2:c.144+15505_144+15506delinsTA NP_001257998.1:n.144+15505_144+15506delinsTA
NM_197957.4:c.171+15505_171+15506delinsTA NP_932061.1:n.171+15505_171+15506delinsTA