Canonical Allele Identifier: CA2142951474

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076201A= , CM000676.2:g.65076201A=	GRCh38
NC_000014.8:g.65542919A= , CM000676.1:g.65542919A=	GRCh37
NC_000014.7:g.64612672A=	NCBI36
NG_029830.1:g.31309T= , LRG_530:g.31309T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*275T=	ENSP00000452206.2:n.*275T=
ENST00000556979.6:c.*1211T=	ENSP00000452378.1:n.*1211T=
ENST00000358664.9:c.*275T= MANE Select	ENSP00000351490.4:n.*275T=
ENST00000651648.1:c.145-5832T=	ENSP00000498863.1:n.145-5832T=
ENST00000284165.10:c.*1602T=	ENSP00000284165.6:n.*1602T=
ENST00000341653.6:c.171+17507T=	ENSP00000342482.2:n.171+17507T=
ENST00000358402.8:c.*275T=	ENSP00000351175.4:n.*275T=
ENST00000358664.8:c.*275T=	ENSP00000351490.4:n.*275T=
ENST00000394606.6:c.*531T=	ENSP00000378104.2:n.*531T=
ENST00000555419.5:c.650T=	ENSP00000452405.1:n.650T=
ENST00000555932.5:c.*250T=	ENSP00000450763.1:n.*250T=
ENST00000618858.4:c.*547T=	ENSP00000480127.1:n.*547T=
NM_001271069.1:c.144+17507T=	NP_001257998.1:n.144+17507T=
NM_002382.4:c.*275T=	NP_002373.3:n.*275T=
NM_145112.2:c.*275T=	NP_660087.1:n.*275T=
NM_145113.2:c.*547T=	NP_660088.1:n.*547T=
NM_197957.3:c.171+17507T=	NP_932061.1:n.171+17507T=
NR_073137.1:n.882T=
XR_429315.2:n.1045T=
NM_001320415.1:c.*275T=	NP_001307344.1:n.*275T=
XM_017021312.2:c.*275T=	XP_016876801.1:n.*275T=
XM_017021313.1:c.*275T=	XP_016876802.1:n.*275T=
XR_001750326.2:n.1103T=
XR_001750327.2:n.1022T=
XR_002957553.1:n.1536T=
XR_943450.3:n.1126T=
XR_943451.3:n.1142T=
XR_943452.3:n.1087T=
NM_001320415.2:c.*275T=	NP_001307344.1:n.*275T=
NM_002382.5:c.*275T= MANE Select	NP_002373.3:n.*275T=
NM_145112.3:c.*275T=	NP_660087.1:n.*275T=
NM_145113.3:c.*547T=	NP_660088.1:n.*547T=
NM_001271069.2:c.144+17507T=	NP_001257998.1:n.144+17507T=
NM_197957.4:c.171+17507T=	NP_932061.1:n.171+17507T=