Canonical Allele Identifier: CA2142951582

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076417G= , CM000676.2:g.65076417G=	GRCh38
NC_000014.8:g.65543135G= , CM000676.1:g.65543135G=	GRCh37
NC_000014.7:g.64612888G=	NCBI36
NG_029830.1:g.31093C= , LRG_530:g.31093C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*59C=	ENSP00000452206.2:n.*59C=
ENST00000556979.6:c.*995C=	ENSP00000452378.1:n.*995C=
ENST00000358664.9:c.*59C= MANE Select	ENSP00000351490.4:n.*59C=
ENST00000651648.1:c.145-6048C=	ENSP00000498863.1:n.145-6048C=
ENST00000284165.10:c.*1386C=	ENSP00000284165.6:n.*1386C=
ENST00000341653.6:c.171+17291C=	ENSP00000342482.2:n.171+17291C=
ENST00000358402.8:c.*59C=	ENSP00000351175.4:n.*59C=
ENST00000358664.8:c.*59C=	ENSP00000351490.4:n.*59C=
ENST00000394606.6:c.*315C=	ENSP00000378104.2:n.*315C=
ENST00000555419.5:c.434C=	ENSP00000452405.1:n.434C=
ENST00000555932.5:c.*34C=	ENSP00000450763.1:n.*34C=
ENST00000618858.4:c.*331C=	ENSP00000480127.1:n.*331C=
NM_001271069.1:c.144+17291C=	NP_001257998.1:n.144+17291C=
NM_002382.4:c.*59C=	NP_002373.3:n.*59C=
NM_145112.2:c.*59C=	NP_660087.1:n.*59C=
NM_145113.2:c.*331C=	NP_660088.1:n.*331C=
NM_197957.3:c.171+17291C=	NP_932061.1:n.171+17291C=
NR_073137.1:n.666C=
XR_429315.2:n.829C=
NM_001320415.1:c.*59C=	NP_001307344.1:n.*59C=
XM_017021312.2:c.*59C=	XP_016876801.1:n.*59C=
XM_017021313.1:c.*59C=	XP_016876802.1:n.*59C=
XR_001750326.2:n.887C=
XR_001750327.2:n.806C=
XR_002957553.1:n.1320C=
XR_943450.3:n.910C=
XR_943451.3:n.926C=
XR_943452.3:n.871C=
NM_001320415.2:c.*59C=	NP_001307344.1:n.*59C=
NM_002382.5:c.*59C= MANE Select	NP_002373.3:n.*59C=
NM_145112.3:c.*59C=	NP_660087.1:n.*59C=
NM_145113.3:c.*331C=	NP_660088.1:n.*331C=
NM_001271069.2:c.144+17291C=	NP_001257998.1:n.144+17291C=
NM_197957.4:c.171+17291C=	NP_932061.1:n.171+17291C=