Canonical Allele Identifier: CA707784326

Gene: MAX

Linked Data

• dbSNP Id: rs1472038026
• gnomAD v3: 14-65075581-C-CT
• gnomAD v4: 14-65075581-C-CT
• MyVariant Identifiers: chr14:g.65542299_65542300insT (hg19) ; chr14:g.65075581_65075582insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075581_65075582insT , CM000676.2:g.65075581_65075582insT	GRCh38
NC_000014.8:g.65542299_65542300insT , CM000676.1:g.65542299_65542300insT	GRCh37
NC_000014.7:g.64612052_64612053insT	NCBI36
NG_029830.1:g.31928_31929insA , LRG_530:g.31928_31929insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*894_*895insA	ENSP00000452206.2:n.*894_*895insA
ENST00000556979.6:c.*1830_*1831insA	ENSP00000452378.1:n.*1830_*1831insA
ENST00000358664.9:c.*894_*895insA MANE Select	ENSP00000351490.4:n.*894_*895insA
ENST00000651648.1:c.145-5213_145-5212insA	ENSP00000498863.1:n.145-5213_145-5212insA
ENST00000284165.10:c.*2221_*2222insA	ENSP00000284165.6:n.*2221_*2222insA
ENST00000341653.6:c.171+18126_171+18127insA	ENSP00000342482.2:n.171+18126_171+18127insA
ENST00000358402.8:c.*894_*895insA	ENSP00000351175.4:n.*894_*895insA
ENST00000358664.8:c.*894_*895insA	ENSP00000351490.4:n.*894_*895insA
ENST00000394606.6:c.*1150_*1151insA	ENSP00000378104.2:n.*1150_*1151insA
ENST00000555932.5:c.*869_*870insA	ENSP00000450763.1:n.*869_*870insA
ENST00000618858.4:c.*1166_*1167insA	ENSP00000480127.1:n.*1166_*1167insA
NM_001271069.1:c.144+18126_144+18127insA	NP_001257998.1:n.144+18126_144+18127insA
NM_002382.4:c.*894_*895insA	NP_002373.3:n.*894_*895insA
NM_145112.2:c.*894_*895insA	NP_660087.1:n.*894_*895insA
NM_145113.2:c.*1166_*1167insA	NP_660088.1:n.*1166_*1167insA
NM_197957.3:c.171+18126_171+18127insA	NP_932061.1:n.171+18126_171+18127insA
NR_073137.1:n.1501_1502insA
XR_429315.2:n.1664_1665insA
NM_001320415.1:c.*894_*895insA	NP_001307344.1:n.*894_*895insA
XM_017021312.2:c.*894_*895insA	XP_016876801.1:n.*894_*895insA
XM_017021313.1:c.*894_*895insA	XP_016876802.1:n.*894_*895insA
XR_001750326.2:n.1722_1723insA
XR_001750327.2:n.1641_1642insA
XR_002957553.1:n.2155_2156insA
XR_943450.3:n.1745_1746insA
XR_943451.3:n.1761_1762insA
XR_943452.3:n.1706_1707insA
NM_001320415.2:c.*894_*895insA	NP_001307344.1:n.*894_*895insA
NM_002382.5:c.*894_*895insA MANE Select	NP_002373.3:n.*894_*895insA
NM_145112.3:c.*894_*895insA	NP_660087.1:n.*894_*895insA
NM_145113.3:c.*1166_*1167insA	NP_660088.1:n.*1166_*1167insA
NM_001271069.2:c.144+18126_144+18127insA	NP_001257998.1:n.144+18126_144+18127insA
NM_197957.4:c.171+18126_171+18127insA	NP_932061.1:n.171+18126_171+18127insA