Canonical Allele Identifier: CA2142951023

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075242A= , CM000676.2:g.65075242A=	GRCh38
NC_000014.8:g.65541960A= , CM000676.1:g.65541960A=	GRCh37
NC_000014.7:g.64611713A=	NCBI36
NG_029830.1:g.32268T= , LRG_530:g.32268T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2170T=	ENSP00000452378.1:n.*2170T=
ENST00000358664.9:c.*1234T= MANE Select	ENSP00000351490.4:n.*1234T=
ENST00000651648.1:c.145-4873T=	ENSP00000498863.1:n.145-4873T=
ENST00000284165.10:c.*2561T=	ENSP00000284165.6:n.*2561T=
ENST00000341653.6:c.171+18466T=	ENSP00000342482.2:n.171+18466T=
ENST00000358402.8:c.*1234T=	ENSP00000351175.4:n.*1234T=
ENST00000394606.6:c.*1490T=	ENSP00000378104.2:n.*1490T=
ENST00000555932.5:c.*1209T=	ENSP00000450763.1:n.*1209T=
ENST00000618858.4:c.*1506T=	ENSP00000480127.1:n.*1506T=
NM_001271069.1:c.144+18466T=	NP_001257998.1:n.144+18466T=
NM_002382.4:c.*1234T=	NP_002373.3:n.*1234T=
NM_145112.2:c.*1234T=	NP_660087.1:n.*1234T=
NM_145113.2:c.*1506T=	NP_660088.1:n.*1506T=
NM_197957.3:c.171+18466T=	NP_932061.1:n.171+18466T=
NR_073137.1:n.1841T=
XR_429315.2:n.2004T=
NM_001320415.1:c.*1234T=	NP_001307344.1:n.*1234T=
XM_017021312.2:c.*1234T=	XP_016876801.1:n.*1234T=
XM_017021313.1:c.*1234T=	XP_016876802.1:n.*1234T=
XR_001750326.2:n.2062T=
XR_001750327.2:n.1981T=
XR_002957553.1:n.2495T=
XR_943450.3:n.2085T=
XR_943451.3:n.2101T=
XR_943452.3:n.2046T=
NM_001320415.2:c.*1234T=	NP_001307344.1:n.*1234T=
NM_002382.5:c.*1234T= MANE Select	NP_002373.3:n.*1234T=
NM_145112.3:c.*1234T=	NP_660087.1:n.*1234T=
NM_145113.3:c.*1506T=	NP_660088.1:n.*1506T=
NM_001271069.2:c.144+18466T=	NP_001257998.1:n.144+18466T=
NM_197957.4:c.171+18466T=	NP_932061.1:n.171+18466T=