Canonical Allele Identifier: CA964079308

Gene: MAX

Linked Data

• dbSNP Id: rs2063026357
• gnomAD v3: 14-65075162-TA-T
• gnomAD v4: 14-65075162-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075165del , CM000676.2:g.65075165del	GRCh38
NC_000014.8:g.65541883del , CM000676.1:g.65541883del	GRCh37
NC_000014.7:g.64611636del	NCBI36
NG_029830.1:g.32347del , LRG_530:g.32347del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2249del	ENSP00000452378.1:n.*2249del
ENST00000358664.9:c.*1313del MANE Select	ENSP00000351490.4:n.*1313del
ENST00000651648.1:c.145-4794del	ENSP00000498863.1:n.145-4794del
ENST00000341653.6:c.171+18545del	ENSP00000342482.2:n.171+18545del
ENST00000358402.8:c.*1313del	ENSP00000351175.4:n.*1313del
ENST00000394606.6:c.*1569del	ENSP00000378104.2:n.*1569del
ENST00000555932.5:c.*1288del	ENSP00000450763.1:n.*1288del
ENST00000618858.4:c.*1585del	ENSP00000480127.1:n.*1585del
NM_001271069.1:c.144+18545del	NP_001257998.1:n.144+18545del
NM_002382.4:c.*1313del	NP_002373.3:n.*1313del
NM_145112.2:c.*1313del	NP_660087.1:n.*1313del
NM_145113.2:c.*1585del	NP_660088.1:n.*1585del
NM_197957.3:c.171+18545del	NP_932061.1:n.171+18545del
NR_073137.1:n.1920del
XR_429315.2:n.2083del
NM_001320415.1:c.*1313del	NP_001307344.1:n.*1313del
XM_017021312.2:c.*1313del	XP_016876801.1:n.*1313del
XM_017021313.1:c.*1313del	XP_016876802.1:n.*1313del
XR_001750326.2:n.2141del
XR_001750327.2:n.2060del
XR_002957553.1:n.2574del
XR_943450.3:n.2164del
XR_943451.3:n.2180del
XR_943452.3:n.2125del
NM_001320415.2:c.*1313del	NP_001307344.1:n.*1313del
NM_002382.5:c.*1313del MANE Select	NP_002373.3:n.*1313del
NM_145112.3:c.*1313del	NP_660087.1:n.*1313del
NM_145113.3:c.*1585del	NP_660088.1:n.*1585del
NM_001271069.2:c.144+18545del	NP_001257998.1:n.144+18545del
NM_197957.4:c.171+18545del	NP_932061.1:n.171+18545del