Canonical Allele Identifier: CA2142951590

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076440A= , CM000676.2:g.65076440A=	GRCh38
NC_000014.8:g.65543158A= , CM000676.1:g.65543158A=	GRCh37
NC_000014.7:g.64612911A=	NCBI36
NG_029830.1:g.31070T= , LRG_530:g.31070T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*36T=	ENSP00000452206.2:n.*36T=
ENST00000556979.6:c.*972T=	ENSP00000452378.1:n.*972T=
ENST00000358664.9:c.*36T= MANE Select	ENSP00000351490.4:n.*36T=
ENST00000651648.1:c.145-6071T=	ENSP00000498863.1:n.145-6071T=
ENST00000284165.10:c.*1363T=	ENSP00000284165.6:n.*1363T=
ENST00000341653.6:c.171+17268T=	ENSP00000342482.2:n.171+17268T=
ENST00000358402.8:c.*36T=	ENSP00000351175.4:n.*36T=
ENST00000358664.8:c.*36T=	ENSP00000351490.4:n.*36T=
ENST00000394606.6:c.*292T=	ENSP00000378104.2:n.*292T=
ENST00000555419.5:c.411T=	ENSP00000452405.1:n.411T=
ENST00000555932.5:c.*11T=	ENSP00000450763.1:n.*11T=
ENST00000618858.4:c.*308T=	ENSP00000480127.1:n.*308T=
NM_001271069.1:c.144+17268T=	NP_001257998.1:n.144+17268T=
NM_002382.4:c.*36T=	NP_002373.3:n.*36T=
NM_145112.2:c.*36T=	NP_660087.1:n.*36T=
NM_145113.2:c.*308T=	NP_660088.1:n.*308T=
NM_197957.3:c.171+17268T=	NP_932061.1:n.171+17268T=
NR_073137.1:n.643T=
XR_429315.2:n.806T=
NM_001320415.1:c.*36T=	NP_001307344.1:n.*36T=
XM_017021312.2:c.*36T=	XP_016876801.1:n.*36T=
XM_017021313.1:c.*36T=	XP_016876802.1:n.*36T=
XR_001750326.2:n.864T=
XR_001750327.2:n.783T=
XR_002957553.1:n.1297T=
XR_943450.3:n.887T=
XR_943451.3:n.903T=
XR_943452.3:n.848T=
NM_001320415.2:c.*36T=	NP_001307344.1:n.*36T=
NM_002382.5:c.*36T= MANE Select	NP_002373.3:n.*36T=
NM_145112.3:c.*36T=	NP_660087.1:n.*36T=
NM_145113.3:c.*308T=	NP_660088.1:n.*308T=
NM_001271069.2:c.144+17268T=	NP_001257998.1:n.144+17268T=
NM_197957.4:c.171+17268T=	NP_932061.1:n.171+17268T=