Canonical Allele Identifier: CA2142951392

Gene: MAX

Linked Data

• dbSNP Id: rs2063048022

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076039_65076040insCC , CM000676.2:g.65076039_65076040insCC	GRCh38
NC_000014.8:g.65542757_65542758insCC , CM000676.1:g.65542757_65542758insCC	GRCh37
NC_000014.7:g.64612510_64612511insCC	NCBI36
NG_029830.1:g.31470_31471insGG , LRG_530:g.31470_31471insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*436_*437insGG	ENSP00000452206.2:n.*436_*437insGG
ENST00000556979.6:c.*1372_*1373insGG	ENSP00000452378.1:n.*1372_*1373insGG
ENST00000358664.9:c.*436_*437insGG MANE Select	ENSP00000351490.4:n.*436_*437insGG
ENST00000651648.1:c.145-5671_145-5670insGG	ENSP00000498863.1:n.145-5671_145-5670insGG
ENST00000284165.10:c.*1763_*1764insGG	ENSP00000284165.6:n.*1763_*1764insGG
ENST00000341653.6:c.171+17668_171+17669insGG	ENSP00000342482.2:n.171+17668_171+17669insGG
ENST00000358402.8:c.*436_*437insGG	ENSP00000351175.4:n.*436_*437insGG
ENST00000358664.8:c.*436_*437insGG	ENSP00000351490.4:n.*436_*437insGG
ENST00000394606.6:c.*692_*693insGG	ENSP00000378104.2:n.*692_*693insGG
ENST00000555932.5:c.*411_*412insGG	ENSP00000450763.1:n.*411_*412insGG
ENST00000618858.4:c.*708_*709insGG	ENSP00000480127.1:n.*708_*709insGG
NM_001271069.1:c.144+17668_144+17669insGG	NP_001257998.1:n.144+17668_144+17669insGG
NM_002382.4:c.*436_*437insGG	NP_002373.3:n.*436_*437insGG
NM_145112.2:c.*436_*437insGG	NP_660087.1:n.*436_*437insGG
NM_145113.2:c.*708_*709insGG	NP_660088.1:n.*708_*709insGG
NM_197957.3:c.171+17668_171+17669insGG	NP_932061.1:n.171+17668_171+17669insGG
NR_073137.1:n.1043_1044insGG
XR_429315.2:n.1206_1207insGG
NM_001320415.1:c.*436_*437insGG	NP_001307344.1:n.*436_*437insGG
XM_017021312.2:c.*436_*437insGG	XP_016876801.1:n.*436_*437insGG
XM_017021313.1:c.*436_*437insGG	XP_016876802.1:n.*436_*437insGG
XR_001750326.2:n.1264_1265insGG
XR_001750327.2:n.1183_1184insGG
XR_002957553.1:n.1697_1698insGG
XR_943450.3:n.1287_1288insGG
XR_943451.3:n.1303_1304insGG
XR_943452.3:n.1248_1249insGG
NM_001320415.2:c.*436_*437insGG	NP_001307344.1:n.*436_*437insGG
NM_002382.5:c.*436_*437insGG MANE Select	NP_002373.3:n.*436_*437insGG
NM_145112.3:c.*436_*437insGG	NP_660087.1:n.*436_*437insGG
NM_145113.3:c.*708_*709insGG	NP_660088.1:n.*708_*709insGG
NM_001271069.2:c.144+17668_144+17669insGG	NP_001257998.1:n.144+17668_144+17669insGG
NM_197957.4:c.171+17668_171+17669insGG	NP_932061.1:n.171+17668_171+17669insGG