Canonical Allele Identifier: CA2625289540

Gene: MAX

Linked Data

• gnomAD v4: 14-65076103-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076108del , CM000676.2:g.65076108del	GRCh38
NC_000014.8:g.65542826del , CM000676.1:g.65542826del	GRCh37
NC_000014.7:g.64612579del	NCBI36
NG_029830.1:g.31406del , LRG_530:g.31406del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*372del	ENSP00000452206.2:n.*372del
ENST00000556979.6:c.*1308del	ENSP00000452378.1:n.*1308del
ENST00000358664.9:c.*372del MANE Select	ENSP00000351490.4:n.*372del
ENST00000651648.1:c.145-5735del	ENSP00000498863.1:n.145-5735del
ENST00000284165.10:c.*1699del	ENSP00000284165.6:n.*1699del
ENST00000341653.6:c.171+17604del	ENSP00000342482.2:n.171+17604del
ENST00000358402.8:c.*372del	ENSP00000351175.4:n.*372del
ENST00000358664.8:c.*372del	ENSP00000351490.4:n.*372del
ENST00000394606.6:c.*628del	ENSP00000378104.2:n.*628del
ENST00000555419.5:c.747del	ENSP00000452405.1:n.747del
ENST00000555932.5:c.*347del	ENSP00000450763.1:n.*347del
ENST00000618858.4:c.*644del	ENSP00000480127.1:n.*644del
NM_001271069.1:c.144+17604del	NP_001257998.1:n.144+17604del
NM_002382.4:c.*372del	NP_002373.3:n.*372del
NM_145112.2:c.*372del	NP_660087.1:n.*372del
NM_145113.2:c.*644del	NP_660088.1:n.*644del
NM_197957.3:c.171+17604del	NP_932061.1:n.171+17604del
NR_073137.1:n.979del
XR_429315.2:n.1142del
NM_001320415.1:c.*372del	NP_001307344.1:n.*372del
XM_017021312.2:c.*372del	XP_016876801.1:n.*372del
XM_017021313.1:c.*372del	XP_016876802.1:n.*372del
XR_001750326.2:n.1200del
XR_001750327.2:n.1119del
XR_002957553.1:n.1633del
XR_943450.3:n.1223del
XR_943451.3:n.1239del
XR_943452.3:n.1184del
NM_001320415.2:c.*372del	NP_001307344.1:n.*372del
NM_002382.5:c.*372del MANE Select	NP_002373.3:n.*372del
NM_145112.3:c.*372del	NP_660087.1:n.*372del
NM_145113.3:c.*644del	NP_660088.1:n.*644del
NM_001271069.2:c.144+17604del	NP_001257998.1:n.144+17604del
NM_197957.4:c.171+17604del	NP_932061.1:n.171+17604del