Canonical Allele Identifier: CA2625289582

Gene: MAX

Linked Data

• gnomAD v4: 14-65076132-AGGAGCTGGTAGGGTGGGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076133_65076150del , CM000676.2:g.65076133_65076150del	GRCh38
NC_000014.8:g.65542851_65542868del , CM000676.1:g.65542851_65542868del	GRCh37
NC_000014.7:g.64612604_64612621del	NCBI36
NG_029830.1:g.31360_31377del , LRG_530:g.31360_31377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*326_*343del	ENSP00000452206.2:n.*326_*343del
ENST00000556979.6:c.*1262_*1279del	ENSP00000452378.1:n.*1262_*1279del
ENST00000358664.9:c.*326_*343del MANE Select	ENSP00000351490.4:n.*326_*343del
ENST00000651648.1:c.145-5781_145-5764del	ENSP00000498863.1:n.145-5781_145-5764del
ENST00000284165.10:c.*1653_*1670del	ENSP00000284165.6:n.*1653_*1670del
ENST00000341653.6:c.171+17558_171+17575del	ENSP00000342482.2:n.171+17558_171+17575del
ENST00000358402.8:c.*326_*343del	ENSP00000351175.4:n.*326_*343del
ENST00000358664.8:c.*326_*343del	ENSP00000351490.4:n.*326_*343del
ENST00000394606.6:c.*582_*599del	ENSP00000378104.2:n.*582_*599del
ENST00000555419.5:c.701_718del	ENSP00000452405.1:n.701_718del
ENST00000555932.5:c.*301_*318del	ENSP00000450763.1:n.*301_*318del
ENST00000618858.4:c.*598_*615del	ENSP00000480127.1:n.*598_*615del
NM_001271069.1:c.144+17558_144+17575del	NP_001257998.1:n.144+17558_144+17575del
NM_002382.4:c.*326_*343del	NP_002373.3:n.*326_*343del
NM_145112.2:c.*326_*343del	NP_660087.1:n.*326_*343del
NM_145113.2:c.*598_*615del	NP_660088.1:n.*598_*615del
NM_197957.3:c.171+17558_171+17575del	NP_932061.1:n.171+17558_171+17575del
NR_073137.1:n.933_950del
XR_429315.2:n.1096_1113del
NM_001320415.1:c.*326_*343del	NP_001307344.1:n.*326_*343del
XM_017021312.2:c.*326_*343del	XP_016876801.1:n.*326_*343del
XM_017021313.1:c.*326_*343del	XP_016876802.1:n.*326_*343del
XR_001750326.2:n.1154_1171del
XR_001750327.2:n.1073_1090del
XR_002957553.1:n.1587_1604del
XR_943450.3:n.1177_1194del
XR_943451.3:n.1193_1210del
XR_943452.3:n.1138_1155del
NM_001320415.2:c.*326_*343del	NP_001307344.1:n.*326_*343del
NM_002382.5:c.*326_*343del MANE Select	NP_002373.3:n.*326_*343del
NM_145112.3:c.*326_*343del	NP_660087.1:n.*326_*343del
NM_145113.3:c.*598_*615del	NP_660088.1:n.*598_*615del
NM_001271069.2:c.144+17558_144+17575del	NP_001257998.1:n.144+17558_144+17575del
NM_197957.4:c.171+17558_171+17575del	NP_932061.1:n.171+17558_171+17575del