Canonical Allele Identifier: CA2625289198

Gene: MAX

Linked Data

• gnomAD v4: 14-65075811-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075812del , CM000676.2:g.65075812del	GRCh38
NC_000014.8:g.65542530del , CM000676.1:g.65542530del	GRCh37
NC_000014.7:g.64612283del	NCBI36
NG_029830.1:g.31698del , LRG_530:g.31698del

Transcript Alleles

HGVS	Amino-acid change
ENST00000556892.6:c.*664del	ENSP00000452206.2:n.*664del
ENST00000556979.6:c.*1600del	ENSP00000452378.1:n.*1600del
ENST00000358664.9:c.*664del MANE Select	ENSP00000351490.4:n.*664del
ENST00000651648.1:c.145-5443del	ENSP00000498863.1:n.145-5443del
ENST00000284165.10:c.*1991del	ENSP00000284165.6:n.*1991del
ENST00000341653.6:c.171+17896del	ENSP00000342482.2:n.171+17896del
ENST00000358402.8:c.*664del	ENSP00000351175.4:n.*664del
ENST00000358664.8:c.*664del	ENSP00000351490.4:n.*664del
ENST00000394606.6:c.*920del	ENSP00000378104.2:n.*920del
ENST00000555932.5:c.*639del	ENSP00000450763.1:n.*639del
ENST00000618858.4:c.*936del	ENSP00000480127.1:n.*936del
NM_001271069.1:c.144+17896del	NP_001257998.1:n.144+17896del
NM_002382.4:c.*664del	NP_002373.3:n.*664del
NM_145112.2:c.*664del	NP_660087.1:n.*664del
NM_145113.2:c.*936del	NP_660088.1:n.*936del
NM_197957.3:c.171+17896del	NP_932061.1:n.171+17896del
NR_073137.1:n.1271del
XR_429315.2:n.1434del
NM_001320415.1:c.*664del	NP_001307344.1:n.*664del
XM_017021312.2:c.*664del	XP_016876801.1:n.*664del
XM_017021313.1:c.*664del	XP_016876802.1:n.*664del
XR_001750326.2:n.1492del
XR_001750327.2:n.1411del
XR_002957553.1:n.1925del
XR_943450.3:n.1515del
XR_943451.3:n.1531del
XR_943452.3:n.1476del
NM_001320415.2:c.*664del	NP_001307344.1:n.*664del
NM_002382.5:c.*664del MANE Select	NP_002373.3:n.*664del
NM_145112.3:c.*664del	NP_660087.1:n.*664del
NM_145113.3:c.*936del	NP_660088.1:n.*936del
NM_001271069.2:c.144+17896del	NP_001257998.1:n.144+17896del
NM_197957.4:c.171+17896del	NP_932061.1:n.171+17896del