Canonical Allele Identifier: CA2142951453

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076160T= , CM000676.2:g.65076160T=	GRCh38
NC_000014.8:g.65542878T= , CM000676.1:g.65542878T=	GRCh37
NC_000014.7:g.64612631T=	NCBI36
NG_029830.1:g.31350A= , LRG_530:g.31350A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*316A=	ENSP00000452206.2:n.*316A=
ENST00000556979.6:c.*1252A=	ENSP00000452378.1:n.*1252A=
ENST00000358664.9:c.*316A= MANE Select	ENSP00000351490.4:n.*316A=
ENST00000651648.1:c.145-5791A=	ENSP00000498863.1:n.145-5791A=
ENST00000284165.10:c.*1643A=	ENSP00000284165.6:n.*1643A=
ENST00000341653.6:c.171+17548A=	ENSP00000342482.2:n.171+17548A=
ENST00000358402.8:c.*316A=	ENSP00000351175.4:n.*316A=
ENST00000358664.8:c.*316A=	ENSP00000351490.4:n.*316A=
ENST00000394606.6:c.*572A=	ENSP00000378104.2:n.*572A=
ENST00000555419.5:c.691A=	ENSP00000452405.1:n.691A=
ENST00000555932.5:c.*291A=	ENSP00000450763.1:n.*291A=
ENST00000618858.4:c.*588A=	ENSP00000480127.1:n.*588A=
NM_001271069.1:c.144+17548A=	NP_001257998.1:n.144+17548A=
NM_002382.4:c.*316A=	NP_002373.3:n.*316A=
NM_145112.2:c.*316A=	NP_660087.1:n.*316A=
NM_145113.2:c.*588A=	NP_660088.1:n.*588A=
NM_197957.3:c.171+17548A=	NP_932061.1:n.171+17548A=
NR_073137.1:n.923A=
XR_429315.2:n.1086A=
NM_001320415.1:c.*316A=	NP_001307344.1:n.*316A=
XM_017021312.2:c.*316A=	XP_016876801.1:n.*316A=
XM_017021313.1:c.*316A=	XP_016876802.1:n.*316A=
XR_001750326.2:n.1144A=
XR_001750327.2:n.1063A=
XR_002957553.1:n.1577A=
XR_943450.3:n.1167A=
XR_943451.3:n.1183A=
XR_943452.3:n.1128A=
NM_001320415.2:c.*316A=	NP_001307344.1:n.*316A=
NM_002382.5:c.*316A= MANE Select	NP_002373.3:n.*316A=
NM_145112.3:c.*316A=	NP_660087.1:n.*316A=
NM_145113.3:c.*588A=	NP_660088.1:n.*588A=
NM_001271069.2:c.144+17548A=	NP_001257998.1:n.144+17548A=
NM_197957.4:c.171+17548A=	NP_932061.1:n.171+17548A=