Canonical Allele Identifier: CA2142951406

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076071_65076072delinsCG , CM000676.2:g.65076071_65076072delinsCG	GRCh38
NC_000014.8:g.65542789_65542790delinsCG , CM000676.1:g.65542789_65542790delinsCG	GRCh37
NC_000014.7:g.64612542_64612543delinsCG	NCBI36
NG_029830.1:g.31438_31439delinsCG , LRG_530:g.31438_31439delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*404_*405delinsCG	ENSP00000452206.2:n.*404_*405delinsCG
ENST00000556979.6:c.*1340_*1341delinsCG	ENSP00000452378.1:n.*1340_*1341delinsCG
ENST00000358664.9:c.*404_*405delinsCG MANE Select	ENSP00000351490.4:n.*404_*405delinsCG
ENST00000651648.1:c.145-5703_145-5702delinsCG	ENSP00000498863.1:n.145-5703_145-5702delinsCG
ENST00000284165.10:c.*1731_*1732delinsCG	ENSP00000284165.6:n.*1731_*1732delinsCG
ENST00000341653.6:c.171+17636_171+17637delinsCG	ENSP00000342482.2:n.171+17636_171+17637delinsCG
ENST00000358402.8:c.*404_*405delinsCG	ENSP00000351175.4:n.*404_*405delinsCG
ENST00000358664.8:c.*404_*405delinsCG	ENSP00000351490.4:n.*404_*405delinsCG
ENST00000394606.6:c.*660_*661delinsCG	ENSP00000378104.2:n.*660_*661delinsCG
ENST00000555932.5:c.*379_*380delinsCG	ENSP00000450763.1:n.*379_*380delinsCG
ENST00000618858.4:c.*676_*677delinsCG	ENSP00000480127.1:n.*676_*677delinsCG
NM_001271069.1:c.144+17636_144+17637delinsCG	NP_001257998.1:n.144+17636_144+17637delinsCG
NM_002382.4:c.*404_*405delinsCG	NP_002373.3:n.*404_*405delinsCG
NM_145112.2:c.*404_*405delinsCG	NP_660087.1:n.*404_*405delinsCG
NM_145113.2:c.*676_*677delinsCG	NP_660088.1:n.*676_*677delinsCG
NM_197957.3:c.171+17636_171+17637delinsCG	NP_932061.1:n.171+17636_171+17637delinsCG
NR_073137.1:n.1011_1012delinsCG
XR_429315.2:n.1174_1175delinsCG
NM_001320415.1:c.*404_*405delinsCG	NP_001307344.1:n.*404_*405delinsCG
XM_017021312.2:c.*404_*405delinsCG	XP_016876801.1:n.*404_*405delinsCG
XM_017021313.1:c.*404_*405delinsCG	XP_016876802.1:n.*404_*405delinsCG
XR_001750326.2:n.1232_1233delinsCG
XR_001750327.2:n.1151_1152delinsCG
XR_002957553.1:n.1665_1666delinsCG
XR_943450.3:n.1255_1256delinsCG
XR_943451.3:n.1271_1272delinsCG
XR_943452.3:n.1216_1217delinsCG
NM_001320415.2:c.*404_*405delinsCG	NP_001307344.1:n.*404_*405delinsCG
NM_002382.5:c.*404_*405delinsCG MANE Select	NP_002373.3:n.*404_*405delinsCG
NM_145112.3:c.*404_*405delinsCG	NP_660087.1:n.*404_*405delinsCG
NM_145113.3:c.*676_*677delinsCG	NP_660088.1:n.*676_*677delinsCG
NM_001271069.2:c.144+17636_144+17637delinsCG	NP_001257998.1:n.144+17636_144+17637delinsCG
NM_197957.4:c.171+17636_171+17637delinsCG	NP_932061.1:n.171+17636_171+17637delinsCG