Canonical Allele Identifier: CA2142951147

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075536_65075540delinsGAAGA , CM000676.2:g.65075536_65075540delinsGAAGA	GRCh38
NC_000014.8:g.65542254_65542258delinsGAAGA , CM000676.1:g.65542254_65542258delinsGAAGA	GRCh37
NC_000014.7:g.64612007_64612011delinsGAAGA	NCBI36
NG_029830.1:g.31970_31974delinsTCTTC , LRG_530:g.31970_31974delinsTCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*1872_*1876delinsTCTTC	ENSP00000452378.1:n.*1872_*1876delinsTCTTC
ENST00000358664.9:c.*936_*940delinsTCTTC MANE Select	ENSP00000351490.4:n.*936_*940delinsTCTTC
ENST00000651648.1:c.145-5171_145-5167delinsTCTTC	ENSP00000498863.1:n.145-5171_145-5167delinsTCTTC
ENST00000284165.10:c.*2263_*2267delinsTCTTC	ENSP00000284165.6:n.*2263_*2267delinsTCTTC
ENST00000341653.6:c.171+18168_171+18172delinsTCTTC	ENSP00000342482.2:n.171+18168_171+18172delinsTCTTC
ENST00000358402.8:c.*936_*940delinsTCTTC	ENSP00000351175.4:n.*936_*940delinsTCTTC
ENST00000394606.6:c.*1192_*1196delinsTCTTC	ENSP00000378104.2:n.*1192_*1196delinsTCTTC
ENST00000555932.5:c.*911_*915delinsTCTTC	ENSP00000450763.1:n.*911_*915delinsTCTTC
ENST00000618858.4:c.*1208_*1212delinsTCTTC	ENSP00000480127.1:n.*1208_*1212delinsTCTTC
NM_001271069.1:c.144+18168_144+18172delinsTCTTC	NP_001257998.1:n.144+18168_144+18172delinsTCTTC
NM_002382.4:c.*936_*940delinsTCTTC	NP_002373.3:n.*936_*940delinsTCTTC
NM_145112.2:c.*936_*940delinsTCTTC	NP_660087.1:n.*936_*940delinsTCTTC
NM_145113.2:c.*1208_*1212delinsTCTTC	NP_660088.1:n.*1208_*1212delinsTCTTC
NM_197957.3:c.171+18168_171+18172delinsTCTTC	NP_932061.1:n.171+18168_171+18172delinsTCTTC
NR_073137.1:n.1543_1547delinsTCTTC
XR_429315.2:n.1706_1710delinsTCTTC
NM_001320415.1:c.*936_*940delinsTCTTC	NP_001307344.1:n.*936_*940delinsTCTTC
XM_017021312.2:c.*936_*940delinsTCTTC	XP_016876801.1:n.*936_*940delinsTCTTC
XM_017021313.1:c.*936_*940delinsTCTTC	XP_016876802.1:n.*936_*940delinsTCTTC
XR_001750326.2:n.1764_1768delinsTCTTC
XR_001750327.2:n.1683_1687delinsTCTTC
XR_002957553.1:n.2197_2201delinsTCTTC
XR_943450.3:n.1787_1791delinsTCTTC
XR_943451.3:n.1803_1807delinsTCTTC
XR_943452.3:n.1748_1752delinsTCTTC
NM_001320415.2:c.*936_*940delinsTCTTC	NP_001307344.1:n.*936_*940delinsTCTTC
NM_002382.5:c.*936_*940delinsTCTTC MANE Select	NP_002373.3:n.*936_*940delinsTCTTC
NM_145112.3:c.*936_*940delinsTCTTC	NP_660087.1:n.*936_*940delinsTCTTC
NM_145113.3:c.*1208_*1212delinsTCTTC	NP_660088.1:n.*1208_*1212delinsTCTTC
NM_001271069.2:c.144+18168_144+18172delinsTCTTC	NP_001257998.1:n.144+18168_144+18172delinsTCTTC
NM_197957.4:c.171+18168_171+18172delinsTCTTC	NP_932061.1:n.171+18168_171+18172delinsTCTTC