Canonical Allele Identifier: CA2142951661

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076606G= , CM000676.2:g.65076606G=	GRCh38
NC_000014.8:g.65543324G= , CM000676.1:g.65543324G=	GRCh37
NC_000014.7:g.64613077G=	NCBI36
NG_029830.1:g.30904C= , LRG_530:g.30904C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.134C=	ENSP00000452206.2:p.Ser45=
ENST00000556979.6:c.*806C=	ENSP00000452378.1:n.*806C=
ENST00000358664.9:c.353C= MANE Select	ENSP00000351490.4:p.Ser118=
ENST00000651648.1:c.145-6237C=	ENSP00000498863.1:n.145-6237C=
ENST00000284165.10:c.*1197C=	ENSP00000284165.6:n.*1197C=
ENST00000341653.6:c.171+17102C=	ENSP00000342482.2:n.171+17102C=
ENST00000358402.8:c.326C=	ENSP00000351175.4:p.Ser109=
ENST00000358664.8:c.353C=	ENSP00000351490.4:p.Ser118=
ENST00000394606.6:c.*126C=	ENSP00000378104.2:n.*126C=
ENST00000553928.5:c.*142C=	ENSP00000451907.1:n.*142C=
ENST00000555419.5:c.245C=	ENSP00000452405.1:p.Ser82=
ENST00000555932.5:c.94C=	ENSP00000450763.1:p.Gln32=
ENST00000557277.5:c.164C=	ENSP00000450955.1:p.Ser55=
ENST00000618858.4:c.*142C=	ENSP00000480127.1:n.*142C=
NM_001271069.1:c.144+17102C=	NP_001257998.1:n.144+17102C=
NM_002382.4:c.353C=	NP_002373.3:p.Ser118=
NM_145112.2:c.326C=	NP_660087.1:p.Ser109=
NM_145113.2:c.*142C=	NP_660088.1:n.*142C=
NM_197957.3:c.171+17102C=	NP_932061.1:n.171+17102C=
NR_073137.1:n.477C=
XR_429315.2:n.640C=
XR_943450.1:n.721C=
XR_943451.1:n.737C=
XR_943452.1:n.683C=
NM_001320415.1:c.164C=	NP_001307344.1:p.Ser55=
XM_017021312.2:c.164C=	XP_016876801.1:p.Ser55=
XM_017021313.1:c.164C=	XP_016876802.1:p.Ser55=
XR_001750326.2:n.698C=
XR_001750327.2:n.617C=
XR_002957553.1:n.1131C=
XR_943450.3:n.721C=
XR_943451.3:n.737C=
XR_943452.3:n.682C=
NM_001320415.2:c.164C=	NP_001307344.1:p.Ser55=
NM_002382.5:c.353C= MANE Select	NP_002373.3:p.Ser118=
NM_145112.3:c.326C=	NP_660087.1:p.Ser109=
NM_145113.3:c.*142C=	NP_660088.1:n.*142C=
NM_001271069.2:c.144+17102C=	NP_001257998.1:n.144+17102C=
NM_197957.4:c.171+17102C=	NP_932061.1:n.171+17102C=