Canonical Allele Identifier: CA2142951131

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075498_65075503delinsCAAAAT , CM000676.2:g.65075498_65075503delinsCAAAAT	GRCh38
NC_000014.8:g.65542216_65542221delinsCAAAAT , CM000676.1:g.65542216_65542221delinsCAAAAT	GRCh37
NC_000014.7:g.64611969_64611974delinsCAAAAT	NCBI36
NG_029830.1:g.32007_32012delinsATTTTG , LRG_530:g.32007_32012delinsATTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*1909_*1914delinsATTTTG	ENSP00000452378.1:n.*1909_*1914delinsATTTTG
ENST00000358664.9:c.*973_*978delinsATTTTG MANE Select	ENSP00000351490.4:n.*973_*978delinsATTTTG
ENST00000651648.1:c.145-5134_145-5129delinsATTTTG	ENSP00000498863.1:n.145-5134_145-5129delinsATTTTG
ENST00000284165.10:c.*2300_*2305delinsATTTTG	ENSP00000284165.6:n.*2300_*2305delinsATTTTG
ENST00000341653.6:c.171+18205_171+18210delinsATTTTG	ENSP00000342482.2:n.171+18205_171+18210delinsATTTTG
ENST00000358402.8:c.*973_*978delinsATTTTG	ENSP00000351175.4:n.*973_*978delinsATTTTG
ENST00000394606.6:c.*1229_*1234delinsATTTTG	ENSP00000378104.2:n.*1229_*1234delinsATTTTG
ENST00000555932.5:c.*948_*953delinsATTTTG	ENSP00000450763.1:n.*948_*953delinsATTTTG
ENST00000618858.4:c.*1245_*1250delinsATTTTG	ENSP00000480127.1:n.*1245_*1250delinsATTTTG
NM_001271069.1:c.144+18205_144+18210delinsATTTTG	NP_001257998.1:n.144+18205_144+18210delinsATTTTG
NM_002382.4:c.*973_*978delinsATTTTG	NP_002373.3:n.*973_*978delinsATTTTG
NM_145112.2:c.*973_*978delinsATTTTG	NP_660087.1:n.*973_*978delinsATTTTG
NM_145113.2:c.*1245_*1250delinsATTTTG	NP_660088.1:n.*1245_*1250delinsATTTTG
NM_197957.3:c.171+18205_171+18210delinsATTTTG	NP_932061.1:n.171+18205_171+18210delinsATTTTG
NR_073137.1:n.1580_1585delinsATTTTG
XR_429315.2:n.1743_1748delinsATTTTG
NM_001320415.1:c.*973_*978delinsATTTTG	NP_001307344.1:n.*973_*978delinsATTTTG
XM_017021312.2:c.*973_*978delinsATTTTG	XP_016876801.1:n.*973_*978delinsATTTTG
XM_017021313.1:c.*973_*978delinsATTTTG	XP_016876802.1:n.*973_*978delinsATTTTG
XR_001750326.2:n.1801_1806delinsATTTTG
XR_001750327.2:n.1720_1725delinsATTTTG
XR_002957553.1:n.2234_2239delinsATTTTG
XR_943450.3:n.1824_1829delinsATTTTG
XR_943451.3:n.1840_1845delinsATTTTG
XR_943452.3:n.1785_1790delinsATTTTG
NM_001320415.2:c.*973_*978delinsATTTTG	NP_001307344.1:n.*973_*978delinsATTTTG
NM_002382.5:c.*973_*978delinsATTTTG MANE Select	NP_002373.3:n.*973_*978delinsATTTTG
NM_145112.3:c.*973_*978delinsATTTTG	NP_660087.1:n.*973_*978delinsATTTTG
NM_145113.3:c.*1245_*1250delinsATTTTG	NP_660088.1:n.*1245_*1250delinsATTTTG
NM_001271069.2:c.144+18205_144+18210delinsATTTTG	NP_001257998.1:n.144+18205_144+18210delinsATTTTG
NM_197957.4:c.171+18205_171+18210delinsATTTTG	NP_932061.1:n.171+18205_171+18210delinsATTTTG