Canonical Allele Identifier: CA2729681681

Gene: MAX

Linked Data

• dbSNP Id: rs2139732079

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075696_65075698del , CM000676.2:g.65075696_65075698del	GRCh38
NC_000014.8:g.65542414_65542416del , CM000676.1:g.65542414_65542416del	GRCh37
NC_000014.7:g.64612167_64612169del	NCBI36
NG_029830.1:g.31813_31815del , LRG_530:g.31813_31815del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*779_*781del	ENSP00000452206.2:n.*779_*781del
ENST00000556979.6:c.*1715_*1717del	ENSP00000452378.1:n.*1715_*1717del
ENST00000358664.9:c.*779_*781del MANE Select	ENSP00000351490.4:n.*779_*781del
ENST00000651648.1:c.145-5328_145-5326del	ENSP00000498863.1:n.145-5328_145-5326del
ENST00000284165.10:c.*2106_*2108del	ENSP00000284165.6:n.*2106_*2108del
ENST00000341653.6:c.171+18011_171+18013del	ENSP00000342482.2:n.171+18011_171+18013del
ENST00000358402.8:c.*779_*781del	ENSP00000351175.4:n.*779_*781del
ENST00000358664.8:c.*779_*781del	ENSP00000351490.4:n.*779_*781del
ENST00000394606.6:c.*1035_*1037del	ENSP00000378104.2:n.*1035_*1037del
ENST00000555932.5:c.*754_*756del	ENSP00000450763.1:n.*754_*756del
ENST00000618858.4:c.*1051_*1053del	ENSP00000480127.1:n.*1051_*1053del
NM_001271069.1:c.144+18011_144+18013del	NP_001257998.1:n.144+18011_144+18013del
NM_002382.4:c.*779_*781del	NP_002373.3:n.*779_*781del
NM_145112.2:c.*779_*781del	NP_660087.1:n.*779_*781del
NM_145113.2:c.*1051_*1053del	NP_660088.1:n.*1051_*1053del
NM_197957.3:c.171+18011_171+18013del	NP_932061.1:n.171+18011_171+18013del
NR_073137.1:n.1386_1388del
XR_429315.2:n.1549_1551del
NM_001320415.1:c.*779_*781del	NP_001307344.1:n.*779_*781del
XM_017021312.2:c.*779_*781del	XP_016876801.1:n.*779_*781del
XM_017021313.1:c.*779_*781del	XP_016876802.1:n.*779_*781del
XR_001750326.2:n.1607_1609del
XR_001750327.2:n.1526_1528del
XR_002957553.1:n.2040_2042del
XR_943450.3:n.1630_1632del
XR_943451.3:n.1646_1648del
XR_943452.3:n.1591_1593del
NM_001320415.2:c.*779_*781del	NP_001307344.1:n.*779_*781del
NM_002382.5:c.*779_*781del MANE Select	NP_002373.3:n.*779_*781del
NM_145112.3:c.*779_*781del	NP_660087.1:n.*779_*781del
NM_145113.3:c.*1051_*1053del	NP_660088.1:n.*1051_*1053del
NM_001271069.2:c.144+18011_144+18013del	NP_001257998.1:n.144+18011_144+18013del
NM_197957.4:c.171+18011_171+18013del	NP_932061.1:n.171+18011_171+18013del