Canonical Allele Identifier: CA2142951235

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075715_65075716delinsAC , CM000676.2:g.65075715_65075716delinsAC	GRCh38
NC_000014.8:g.65542433_65542434delinsAC , CM000676.1:g.65542433_65542434delinsAC	GRCh37
NC_000014.7:g.64612186_64612187delinsAC	NCBI36
NG_029830.1:g.31794_31795delinsGT , LRG_530:g.31794_31795delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*760_*761delinsGT	ENSP00000452206.2:n.*760_*761delinsGT
ENST00000556979.6:c.*1696_*1697delinsGT	ENSP00000452378.1:n.*1696_*1697delinsGT
ENST00000358664.9:c.*760_*761delinsGT MANE Select	ENSP00000351490.4:n.*760_*761delinsGT
ENST00000651648.1:c.145-5347_145-5346delinsGT	ENSP00000498863.1:n.145-5347_145-5346delinsGT
ENST00000284165.10:c.*2087_*2088delinsGT	ENSP00000284165.6:n.*2087_*2088delinsGT
ENST00000341653.6:c.171+17992_171+17993delinsGT	ENSP00000342482.2:n.171+17992_171+17993delinsGT
ENST00000358402.8:c.*760_*761delinsGT	ENSP00000351175.4:n.*760_*761delinsGT
ENST00000358664.8:c.*760_*761delinsGT	ENSP00000351490.4:n.*760_*761delinsGT
ENST00000394606.6:c.*1016_*1017delinsGT	ENSP00000378104.2:n.*1016_*1017delinsGT
ENST00000555932.5:c.*735_*736delinsGT	ENSP00000450763.1:n.*735_*736delinsGT
ENST00000618858.4:c.*1032_*1033delinsGT	ENSP00000480127.1:n.*1032_*1033delinsGT
NM_001271069.1:c.144+17992_144+17993delinsGT	NP_001257998.1:n.144+17992_144+17993delinsGT
NM_002382.4:c.*760_*761delinsGT	NP_002373.3:n.*760_*761delinsGT
NM_145112.2:c.*760_*761delinsGT	NP_660087.1:n.*760_*761delinsGT
NM_145113.2:c.*1032_*1033delinsGT	NP_660088.1:n.*1032_*1033delinsGT
NM_197957.3:c.171+17992_171+17993delinsGT	NP_932061.1:n.171+17992_171+17993delinsGT
NR_073137.1:n.1367_1368delinsGT
XR_429315.2:n.1530_1531delinsGT
NM_001320415.1:c.*760_*761delinsGT	NP_001307344.1:n.*760_*761delinsGT
XM_017021312.2:c.*760_*761delinsGT	XP_016876801.1:n.*760_*761delinsGT
XM_017021313.1:c.*760_*761delinsGT	XP_016876802.1:n.*760_*761delinsGT
XR_001750326.2:n.1588_1589delinsGT
XR_001750327.2:n.1507_1508delinsGT
XR_002957553.1:n.2021_2022delinsGT
XR_943450.3:n.1611_1612delinsGT
XR_943451.3:n.1627_1628delinsGT
XR_943452.3:n.1572_1573delinsGT
NM_001320415.2:c.*760_*761delinsGT	NP_001307344.1:n.*760_*761delinsGT
NM_002382.5:c.*760_*761delinsGT MANE Select	NP_002373.3:n.*760_*761delinsGT
NM_145112.3:c.*760_*761delinsGT	NP_660087.1:n.*760_*761delinsGT
NM_145113.3:c.*1032_*1033delinsGT	NP_660088.1:n.*1032_*1033delinsGT
NM_001271069.2:c.144+17992_144+17993delinsGT	NP_001257998.1:n.144+17992_144+17993delinsGT
NM_197957.4:c.171+17992_171+17993delinsGT	NP_932061.1:n.171+17992_171+17993delinsGT