Canonical Allele Identifier: CA2142951658

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076599G= , CM000676.2:g.65076599G=	GRCh38
NC_000014.8:g.65543317G= , CM000676.1:g.65543317G=	GRCh37
NC_000014.7:g.64613070G=	NCBI36
NG_029830.1:g.30911C= , LRG_530:g.30911C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.141C=	ENSP00000452206.2:p.Asn47=
ENST00000556979.6:c.*813C=	ENSP00000452378.1:n.*813C=
ENST00000358664.9:c.360C= MANE Select	ENSP00000351490.4:p.Asn120=
ENST00000651648.1:c.145-6230C=	ENSP00000498863.1:n.145-6230C=
ENST00000284165.10:c.*1204C=	ENSP00000284165.6:n.*1204C=
ENST00000341653.6:c.171+17109C=	ENSP00000342482.2:n.171+17109C=
ENST00000358402.8:c.333C=	ENSP00000351175.4:p.Asn111=
ENST00000358664.8:c.360C=	ENSP00000351490.4:p.Asn120=
ENST00000394606.6:c.*133C=	ENSP00000378104.2:n.*133C=
ENST00000553928.5:c.*149C=	ENSP00000451907.1:n.*149C=
ENST00000555419.5:c.252C=	ENSP00000452405.1:p.Asn84=
ENST00000555932.5:c.101C=	ENSP00000450763.1:p.Thr34=
ENST00000557277.5:c.171C=	ENSP00000450955.1:p.Asn57=
ENST00000618858.4:c.*149C=	ENSP00000480127.1:n.*149C=
NM_001271069.1:c.144+17109C=	NP_001257998.1:n.144+17109C=
NM_002382.4:c.360C=	NP_002373.3:p.Asn120=
NM_145112.2:c.333C=	NP_660087.1:p.Asn111=
NM_145113.2:c.*149C=	NP_660088.1:n.*149C=
NM_197957.3:c.171+17109C=	NP_932061.1:n.171+17109C=
NR_073137.1:n.484C=
XR_429315.2:n.647C=
XR_943450.1:n.728C=
XR_943451.1:n.744C=
XR_943452.1:n.690C=
NM_001320415.1:c.171C=	NP_001307344.1:p.Asn57=
XM_017021312.2:c.171C=	XP_016876801.1:p.Asn57=
XM_017021313.1:c.171C=	XP_016876802.1:p.Asn57=
XR_001750326.2:n.705C=
XR_001750327.2:n.624C=
XR_002957553.1:n.1138C=
XR_943450.3:n.728C=
XR_943451.3:n.744C=
XR_943452.3:n.689C=
NM_001320415.2:c.171C=	NP_001307344.1:p.Asn57=
NM_002382.5:c.360C= MANE Select	NP_002373.3:p.Asn120=
NM_145112.3:c.333C=	NP_660087.1:p.Asn111=
NM_145113.3:c.*149C=	NP_660088.1:n.*149C=
NM_001271069.2:c.144+17109C=	NP_001257998.1:n.144+17109C=
NM_197957.4:c.171+17109C=	NP_932061.1:n.171+17109C=