Canonical Allele Identifier: CA2625289556

Gene: MAX

Linked Data

• gnomAD v4: 14-65076110-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076110_65076111insT , CM000676.2:g.65076110_65076111insT	GRCh38
NC_000014.8:g.65542828_65542829insT , CM000676.1:g.65542828_65542829insT	GRCh37
NC_000014.7:g.64612581_64612582insT	NCBI36
NG_029830.1:g.31399_31400insA , LRG_530:g.31399_31400insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*365_*366insA	ENSP00000452206.2:n.*365_*366insA
ENST00000556979.6:c.*1301_*1302insA	ENSP00000452378.1:n.*1301_*1302insA
ENST00000358664.9:c.*365_*366insA MANE Select	ENSP00000351490.4:n.*365_*366insA
ENST00000651648.1:c.145-5742_145-5741insA	ENSP00000498863.1:n.145-5742_145-5741insA
ENST00000284165.10:c.*1692_*1693insA	ENSP00000284165.6:n.*1692_*1693insA
ENST00000341653.6:c.171+17597_171+17598insA	ENSP00000342482.2:n.171+17597_171+17598insA
ENST00000358402.8:c.*365_*366insA	ENSP00000351175.4:n.*365_*366insA
ENST00000358664.8:c.*365_*366insA	ENSP00000351490.4:n.*365_*366insA
ENST00000394606.6:c.*621_*622insA	ENSP00000378104.2:n.*621_*622insA
ENST00000555419.5:c.740_741insA	ENSP00000452405.1:n.740_741insA
ENST00000555932.5:c.*340_*341insA	ENSP00000450763.1:n.*340_*341insA
ENST00000618858.4:c.*637_*638insA	ENSP00000480127.1:n.*637_*638insA
NM_001271069.1:c.144+17597_144+17598insA	NP_001257998.1:n.144+17597_144+17598insA
NM_002382.4:c.*365_*366insA	NP_002373.3:n.*365_*366insA
NM_145112.2:c.*365_*366insA	NP_660087.1:n.*365_*366insA
NM_145113.2:c.*637_*638insA	NP_660088.1:n.*637_*638insA
NM_197957.3:c.171+17597_171+17598insA	NP_932061.1:n.171+17597_171+17598insA
NR_073137.1:n.972_973insA
XR_429315.2:n.1135_1136insA
NM_001320415.1:c.*365_*366insA	NP_001307344.1:n.*365_*366insA
XM_017021312.2:c.*365_*366insA	XP_016876801.1:n.*365_*366insA
XM_017021313.1:c.*365_*366insA	XP_016876802.1:n.*365_*366insA
XR_001750326.2:n.1193_1194insA
XR_001750327.2:n.1112_1113insA
XR_002957553.1:n.1626_1627insA
XR_943450.3:n.1216_1217insA
XR_943451.3:n.1232_1233insA
XR_943452.3:n.1177_1178insA
NM_001320415.2:c.*365_*366insA	NP_001307344.1:n.*365_*366insA
NM_002382.5:c.*365_*366insA MANE Select	NP_002373.3:n.*365_*366insA
NM_145112.3:c.*365_*366insA	NP_660087.1:n.*365_*366insA
NM_145113.3:c.*637_*638insA	NP_660088.1:n.*637_*638insA
NM_001271069.2:c.144+17597_144+17598insA	NP_001257998.1:n.144+17597_144+17598insA
NM_197957.4:c.171+17597_171+17598insA	NP_932061.1:n.171+17597_171+17598insA