Canonical Allele Identifier: CA2142951614

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076509T= , CM000676.2:g.65076509T=	GRCh38
NC_000014.8:g.65543227T= , CM000676.1:g.65543227T=	GRCh37
NC_000014.7:g.64612980T=	NCBI36
NG_029830.1:g.31001A= , LRG_530:g.31001A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.231A=	ENSP00000452206.2:p.Gln77=
ENST00000556979.6:c.*903A=	ENSP00000452378.1:n.*903A=
ENST00000358664.9:c.450A= MANE Select	ENSP00000351490.4:p.Gln150=
ENST00000651648.1:c.145-6140A=	ENSP00000498863.1:n.145-6140A=
ENST00000284165.10:c.*1294A=	ENSP00000284165.6:n.*1294A=
ENST00000341653.6:c.171+17199A=	ENSP00000342482.2:n.171+17199A=
ENST00000358402.8:c.423A=	ENSP00000351175.4:p.Gln141=
ENST00000358664.8:c.450A=	ENSP00000351490.4:p.Gln150=
ENST00000394606.6:c.*223A=	ENSP00000378104.2:n.*223A=
ENST00000553928.5:c.*239A=	ENSP00000451907.1:n.*239A=
ENST00000555419.5:c.342A=	ENSP00000452405.1:p.Gln114=
ENST00000555932.5:c.191A=	ENSP00000450763.1:p.Lys64=
ENST00000557277.5:c.261A=	ENSP00000450955.1:p.Gln87=
ENST00000618858.4:c.*239A=	ENSP00000480127.1:n.*239A=
NM_001271069.1:c.144+17199A=	NP_001257998.1:n.144+17199A=
NM_002382.4:c.450A=	NP_002373.3:p.Gln150=
NM_145112.2:c.423A=	NP_660087.1:p.Gln141=
NM_145113.2:c.*239A=	NP_660088.1:n.*239A=
NM_197957.3:c.171+17199A=	NP_932061.1:n.171+17199A=
NR_073137.1:n.574A=
XR_429315.2:n.737A=
NM_001320415.1:c.261A=	NP_001307344.1:p.Gln87=
XM_017021312.2:c.261A=	XP_016876801.1:p.Gln87=
XM_017021313.1:c.261A=	XP_016876802.1:p.Gln87=
XR_001750326.2:n.795A=
XR_001750327.2:n.714A=
XR_002957553.1:n.1228A=
XR_943450.3:n.818A=
XR_943451.3:n.834A=
XR_943452.3:n.779A=
NM_001320415.2:c.261A=	NP_001307344.1:p.Gln87=
NM_002382.5:c.450A= MANE Select	NP_002373.3:p.Gln150=
NM_145112.3:c.423A=	NP_660087.1:p.Gln141=
NM_145113.3:c.*239A=	NP_660088.1:n.*239A=
NM_001271069.2:c.144+17199A=	NP_001257998.1:n.144+17199A=
NM_197957.4:c.171+17199A=	NP_932061.1:n.171+17199A=