Canonical Allele Identifier: CA2142951021

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075240_65075241delinsCA , CM000676.2:g.65075240_65075241delinsCA	GRCh38
NC_000014.8:g.65541958_65541959delinsCA , CM000676.1:g.65541958_65541959delinsCA	GRCh37
NC_000014.7:g.64611711_64611712delinsCA	NCBI36
NG_029830.1:g.32269_32270delinsTG , LRG_530:g.32269_32270delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2171_*2172delinsTG	ENSP00000452378.1:n.*2171_*2172delinsTG
ENST00000358664.9:c.*1235_*1236delinsTG MANE Select	ENSP00000351490.4:n.*1235_*1236delinsTG
ENST00000651648.1:c.145-4872_145-4871delinsTG	ENSP00000498863.1:n.145-4872_145-4871delinsTG
ENST00000284165.10:c.*2562_*2563delinsTG	ENSP00000284165.6:n.*2562_*2563delinsTG
ENST00000341653.6:c.171+18467_171+18468delinsTG	ENSP00000342482.2:n.171+18467_171+18468delinsTG
ENST00000358402.8:c.*1235_*1236delinsTG	ENSP00000351175.4:n.*1235_*1236delinsTG
ENST00000394606.6:c.*1491_*1492delinsTG	ENSP00000378104.2:n.*1491_*1492delinsTG
ENST00000555932.5:c.*1210_*1211delinsTG	ENSP00000450763.1:n.*1210_*1211delinsTG
ENST00000618858.4:c.*1507_*1508delinsTG	ENSP00000480127.1:n.*1507_*1508delinsTG
NM_001271069.1:c.144+18467_144+18468delinsTG	NP_001257998.1:n.144+18467_144+18468delinsTG
NM_002382.4:c.*1235_*1236delinsTG	NP_002373.3:n.*1235_*1236delinsTG
NM_145112.2:c.*1235_*1236delinsTG	NP_660087.1:n.*1235_*1236delinsTG
NM_145113.2:c.*1507_*1508delinsTG	NP_660088.1:n.*1507_*1508delinsTG
NM_197957.3:c.171+18467_171+18468delinsTG	NP_932061.1:n.171+18467_171+18468delinsTG
NR_073137.1:n.1842_1843delinsTG
XR_429315.2:n.2005_2006delinsTG
NM_001320415.1:c.*1235_*1236delinsTG	NP_001307344.1:n.*1235_*1236delinsTG
XM_017021312.2:c.*1235_*1236delinsTG	XP_016876801.1:n.*1235_*1236delinsTG
XM_017021313.1:c.*1235_*1236delinsTG	XP_016876802.1:n.*1235_*1236delinsTG
XR_001750326.2:n.2063_2064delinsTG
XR_001750327.2:n.1982_1983delinsTG
XR_002957553.1:n.2496_2497delinsTG
XR_943450.3:n.2086_2087delinsTG
XR_943451.3:n.2102_2103delinsTG
XR_943452.3:n.2047_2048delinsTG
NM_001320415.2:c.*1235_*1236delinsTG	NP_001307344.1:n.*1235_*1236delinsTG
NM_002382.5:c.*1235_*1236delinsTG MANE Select	NP_002373.3:n.*1235_*1236delinsTG
NM_145112.3:c.*1235_*1236delinsTG	NP_660087.1:n.*1235_*1236delinsTG
NM_145113.3:c.*1507_*1508delinsTG	NP_660088.1:n.*1507_*1508delinsTG
NM_001271069.2:c.144+18467_144+18468delinsTG	NP_001257998.1:n.144+18467_144+18468delinsTG
NM_197957.4:c.171+18467_171+18468delinsTG	NP_932061.1:n.171+18467_171+18468delinsTG