Canonical Allele Identifier: CA2625289491

Gene: MAX

Linked Data

• gnomAD v4: 14-65076071-CGGGCCAGGAGGCCACCTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076073_65076091del , CM000676.2:g.65076073_65076091del	GRCh38
NC_000014.8:g.65542791_65542809del , CM000676.1:g.65542791_65542809del	GRCh37
NC_000014.7:g.64612544_64612562del	NCBI36
NG_029830.1:g.31420_31438del , LRG_530:g.31420_31438del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*386_*404del	ENSP00000452206.2:n.*386_*404del
ENST00000556979.6:c.*1322_*1340del	ENSP00000452378.1:n.*1322_*1340del
ENST00000358664.9:c.*386_*404del MANE Select	ENSP00000351490.4:n.*386_*404del
ENST00000651648.1:c.145-5721_145-5703del	ENSP00000498863.1:n.145-5721_145-5703del
ENST00000284165.10:c.*1713_*1731del	ENSP00000284165.6:n.*1713_*1731del
ENST00000341653.6:c.171+17618_171+17636del	ENSP00000342482.2:n.171+17618_171+17636del
ENST00000358402.8:c.*386_*404del	ENSP00000351175.4:n.*386_*404del
ENST00000358664.8:c.*386_*404del	ENSP00000351490.4:n.*386_*404del
ENST00000394606.6:c.*642_*660del	ENSP00000378104.2:n.*642_*660del
ENST00000555932.5:c.*361_*379del	ENSP00000450763.1:n.*361_*379del
ENST00000618858.4:c.*658_*676del	ENSP00000480127.1:n.*658_*676del
NM_001271069.1:c.144+17618_144+17636del	NP_001257998.1:n.144+17618_144+17636del
NM_002382.4:c.*386_*404del	NP_002373.3:n.*386_*404del
NM_145112.2:c.*386_*404del	NP_660087.1:n.*386_*404del
NM_145113.2:c.*658_*676del	NP_660088.1:n.*658_*676del
NM_197957.3:c.171+17618_171+17636del	NP_932061.1:n.171+17618_171+17636del
NR_073137.1:n.993_1011del
XR_429315.2:n.1156_1174del
NM_001320415.1:c.*386_*404del	NP_001307344.1:n.*386_*404del
XM_017021312.2:c.*386_*404del	XP_016876801.1:n.*386_*404del
XM_017021313.1:c.*386_*404del	XP_016876802.1:n.*386_*404del
XR_001750326.2:n.1214_1232del
XR_001750327.2:n.1133_1151del
XR_002957553.1:n.1647_1665del
XR_943450.3:n.1237_1255del
XR_943451.3:n.1253_1271del
XR_943452.3:n.1198_1216del
NM_001320415.2:c.*386_*404del	NP_001307344.1:n.*386_*404del
NM_002382.5:c.*386_*404del MANE Select	NP_002373.3:n.*386_*404del
NM_145112.3:c.*386_*404del	NP_660087.1:n.*386_*404del
NM_145113.3:c.*658_*676del	NP_660088.1:n.*658_*676del
NM_001271069.2:c.144+17618_144+17636del	NP_001257998.1:n.144+17618_144+17636del
NM_197957.4:c.171+17618_171+17636del	NP_932061.1:n.171+17618_171+17636del