Canonical Allele Identifier: CA2142951319

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075864_65075866delinsCTG , CM000676.2:g.65075864_65075866delinsCTG	GRCh38
NC_000014.8:g.65542582_65542584delinsCTG , CM000676.1:g.65542582_65542584delinsCTG	GRCh37
NC_000014.7:g.64612335_64612337delinsCTG	NCBI36
NG_029830.1:g.31644_31646delinsCAG , LRG_530:g.31644_31646delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*610_*612delinsCAG	ENSP00000452206.2:n.*610_*612delinsCAG
ENST00000556979.6:c.*1546_*1548delinsCAG	ENSP00000452378.1:n.*1546_*1548delinsCAG
ENST00000358664.9:c.*610_*612delinsCAG MANE Select	ENSP00000351490.4:n.*610_*612delinsCAG
ENST00000651648.1:c.145-5497_145-5495delinsCAG	ENSP00000498863.1:n.145-5497_145-5495delinsCAG
ENST00000284165.10:c.*1937_*1939delinsCAG	ENSP00000284165.6:n.*1937_*1939delinsCAG
ENST00000341653.6:c.171+17842_171+17844delinsCAG	ENSP00000342482.2:n.171+17842_171+17844delinsCAG
ENST00000358402.8:c.*610_*612delinsCAG	ENSP00000351175.4:n.*610_*612delinsCAG
ENST00000358664.8:c.*610_*612delinsCAG	ENSP00000351490.4:n.*610_*612delinsCAG
ENST00000394606.6:c.*866_*868delinsCAG	ENSP00000378104.2:n.*866_*868delinsCAG
ENST00000555932.5:c.*585_*587delinsCAG	ENSP00000450763.1:n.*585_*587delinsCAG
ENST00000618858.4:c.*882_*884delinsCAG	ENSP00000480127.1:n.*882_*884delinsCAG
NM_001271069.1:c.144+17842_144+17844delinsCAG	NP_001257998.1:n.144+17842_144+17844delinsCAG
NM_002382.4:c.*610_*612delinsCAG	NP_002373.3:n.*610_*612delinsCAG
NM_145112.2:c.*610_*612delinsCAG	NP_660087.1:n.*610_*612delinsCAG
NM_145113.2:c.*882_*884delinsCAG	NP_660088.1:n.*882_*884delinsCAG
NM_197957.3:c.171+17842_171+17844delinsCAG	NP_932061.1:n.171+17842_171+17844delinsCAG
NR_073137.1:n.1217_1219delinsCAG
XR_429315.2:n.1380_1382delinsCAG
NM_001320415.1:c.*610_*612delinsCAG	NP_001307344.1:n.*610_*612delinsCAG
XM_017021312.2:c.*610_*612delinsCAG	XP_016876801.1:n.*610_*612delinsCAG
XM_017021313.1:c.*610_*612delinsCAG	XP_016876802.1:n.*610_*612delinsCAG
XR_001750326.2:n.1438_1440delinsCAG
XR_001750327.2:n.1357_1359delinsCAG
XR_002957553.1:n.1871_1873delinsCAG
XR_943450.3:n.1461_1463delinsCAG
XR_943451.3:n.1477_1479delinsCAG
XR_943452.3:n.1422_1424delinsCAG
NM_001320415.2:c.*610_*612delinsCAG	NP_001307344.1:n.*610_*612delinsCAG
NM_002382.5:c.*610_*612delinsCAG MANE Select	NP_002373.3:n.*610_*612delinsCAG
NM_145112.3:c.*610_*612delinsCAG	NP_660087.1:n.*610_*612delinsCAG
NM_145113.3:c.*882_*884delinsCAG	NP_660088.1:n.*882_*884delinsCAG
NM_001271069.2:c.144+17842_144+17844delinsCAG	NP_001257998.1:n.144+17842_144+17844delinsCAG
NM_197957.4:c.171+17842_171+17844delinsCAG	NP_932061.1:n.171+17842_171+17844delinsCAG