Canonical Allele Identifier: CA2142950996

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075180_65075181delinsCT , CM000676.2:g.65075180_65075181delinsCT	GRCh38
NC_000014.8:g.65541898_65541899delinsCT , CM000676.1:g.65541898_65541899delinsCT	GRCh37
NC_000014.7:g.64611651_64611652delinsCT	NCBI36
NG_029830.1:g.32329_32330delinsAG , LRG_530:g.32329_32330delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2231_*2232delinsAG	ENSP00000452378.1:n.*2231_*2232delinsAG
ENST00000358664.9:c.*1295_*1296delinsAG MANE Select	ENSP00000351490.4:n.*1295_*1296delinsAG
ENST00000651648.1:c.145-4812_145-4811delinsAG	ENSP00000498863.1:n.145-4812_145-4811delinsAG
ENST00000341653.6:c.171+18527_171+18528delinsAG	ENSP00000342482.2:n.171+18527_171+18528delinsAG
ENST00000358402.8:c.*1295_*1296delinsAG	ENSP00000351175.4:n.*1295_*1296delinsAG
ENST00000394606.6:c.*1551_*1552delinsAG	ENSP00000378104.2:n.*1551_*1552delinsAG
ENST00000555932.5:c.*1270_*1271delinsAG	ENSP00000450763.1:n.*1270_*1271delinsAG
ENST00000618858.4:c.*1567_*1568delinsAG	ENSP00000480127.1:n.*1567_*1568delinsAG
NM_001271069.1:c.144+18527_144+18528delinsAG	NP_001257998.1:n.144+18527_144+18528delinsAG
NM_002382.4:c.*1295_*1296delinsAG	NP_002373.3:n.*1295_*1296delinsAG
NM_145112.2:c.*1295_*1296delinsAG	NP_660087.1:n.*1295_*1296delinsAG
NM_145113.2:c.*1567_*1568delinsAG	NP_660088.1:n.*1567_*1568delinsAG
NM_197957.3:c.171+18527_171+18528delinsAG	NP_932061.1:n.171+18527_171+18528delinsAG
NR_073137.1:n.1902_1903delinsAG
XR_429315.2:n.2065_2066delinsAG
NM_001320415.1:c.*1295_*1296delinsAG	NP_001307344.1:n.*1295_*1296delinsAG
XM_017021312.2:c.*1295_*1296delinsAG	XP_016876801.1:n.*1295_*1296delinsAG
XM_017021313.1:c.*1295_*1296delinsAG	XP_016876802.1:n.*1295_*1296delinsAG
XR_001750326.2:n.2123_2124delinsAG
XR_001750327.2:n.2042_2043delinsAG
XR_002957553.1:n.2556_2557delinsAG
XR_943450.3:n.2146_2147delinsAG
XR_943451.3:n.2162_2163delinsAG
XR_943452.3:n.2107_2108delinsAG
NM_001320415.2:c.*1295_*1296delinsAG	NP_001307344.1:n.*1295_*1296delinsAG
NM_002382.5:c.*1295_*1296delinsAG MANE Select	NP_002373.3:n.*1295_*1296delinsAG
NM_145112.3:c.*1295_*1296delinsAG	NP_660087.1:n.*1295_*1296delinsAG
NM_145113.3:c.*1567_*1568delinsAG	NP_660088.1:n.*1567_*1568delinsAG
NM_001271069.2:c.144+18527_144+18528delinsAG	NP_001257998.1:n.144+18527_144+18528delinsAG
NM_197957.4:c.171+18527_171+18528delinsAG	NP_932061.1:n.171+18527_171+18528delinsAG