Canonical Allele Identifier: CA964079530

Gene: MAX

Linked Data

• dbSNP Id: rs2063034885
• gnomAD v3: 14-65075513-CT-C
• gnomAD v4: 14-65075513-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075514del , CM000676.2:g.65075514del	GRCh38
NC_000014.8:g.65542232del , CM000676.1:g.65542232del	GRCh37
NC_000014.7:g.64611985del	NCBI36
NG_029830.1:g.31996del , LRG_530:g.31996del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*1898del	ENSP00000452378.1:n.*1898del
ENST00000358664.9:c.*962del MANE Select	ENSP00000351490.4:n.*962del
ENST00000651648.1:c.145-5145del	ENSP00000498863.1:n.145-5145del
ENST00000284165.10:c.*2289del	ENSP00000284165.6:n.*2289del
ENST00000341653.6:c.171+18194del	ENSP00000342482.2:n.171+18194del
ENST00000358402.8:c.*962del	ENSP00000351175.4:n.*962del
ENST00000394606.6:c.*1218del	ENSP00000378104.2:n.*1218del
ENST00000555932.5:c.*937del	ENSP00000450763.1:n.*937del
ENST00000618858.4:c.*1234del	ENSP00000480127.1:n.*1234del
NM_001271069.1:c.144+18194del	NP_001257998.1:n.144+18194del
NM_002382.4:c.*962del	NP_002373.3:n.*962del
NM_145112.2:c.*962del	NP_660087.1:n.*962del
NM_145113.2:c.*1234del	NP_660088.1:n.*1234del
NM_197957.3:c.171+18194del	NP_932061.1:n.171+18194del
NR_073137.1:n.1569del
XR_429315.2:n.1732del
NM_001320415.1:c.*962del	NP_001307344.1:n.*962del
XM_017021312.2:c.*962del	XP_016876801.1:n.*962del
XM_017021313.1:c.*962del	XP_016876802.1:n.*962del
XR_001750326.2:n.1790del
XR_001750327.2:n.1709del
XR_002957553.1:n.2223del
XR_943450.3:n.1813del
XR_943451.3:n.1829del
XR_943452.3:n.1774del
NM_001320415.2:c.*962del	NP_001307344.1:n.*962del
NM_002382.5:c.*962del MANE Select	NP_002373.3:n.*962del
NM_145112.3:c.*962del	NP_660087.1:n.*962del
NM_145113.3:c.*1234del	NP_660088.1:n.*1234del
NM_001271069.2:c.144+18194del	NP_001257998.1:n.144+18194del
NM_197957.4:c.171+18194del	NP_932061.1:n.171+18194del