Canonical Allele Identifier: CA2142951657

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076598T= , CM000676.2:g.65076598T=	GRCh38
NC_000014.8:g.65543316T= , CM000676.1:g.65543316T=	GRCh37
NC_000014.7:g.64613069T=	NCBI36
NG_029830.1:g.30912A= , LRG_530:g.30912A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.142A=	ENSP00000452206.2:p.Ser48=
ENST00000556979.6:c.*814A=	ENSP00000452378.1:n.*814A=
ENST00000358664.9:c.361A= MANE Select	ENSP00000351490.4:p.Ser121=
ENST00000651648.1:c.145-6229A=	ENSP00000498863.1:n.145-6229A=
ENST00000284165.10:c.*1205A=	ENSP00000284165.6:n.*1205A=
ENST00000341653.6:c.171+17110A=	ENSP00000342482.2:n.171+17110A=
ENST00000358402.8:c.334A=	ENSP00000351175.4:p.Ser112=
ENST00000358664.8:c.361A=	ENSP00000351490.4:p.Ser121=
ENST00000394606.6:c.*134A=	ENSP00000378104.2:n.*134A=
ENST00000553928.5:c.*150A=	ENSP00000451907.1:n.*150A=
ENST00000555419.5:c.253A=	ENSP00000452405.1:p.Ser85=
ENST00000555932.5:c.102A=	ENSP00000450763.1:p.Thr34=
ENST00000557277.5:c.172A=	ENSP00000450955.1:p.Ser58=
ENST00000618858.4:c.*150A=	ENSP00000480127.1:n.*150A=
NM_001271069.1:c.144+17110A=	NP_001257998.1:n.144+17110A=
NM_002382.4:c.361A=	NP_002373.3:p.Ser121=
NM_145112.2:c.334A=	NP_660087.1:p.Ser112=
NM_145113.2:c.*150A=	NP_660088.1:n.*150A=
NM_197957.3:c.171+17110A=	NP_932061.1:n.171+17110A=
NR_073137.1:n.485A=
XR_429315.2:n.648A=
XR_943450.1:n.729A=
XR_943451.1:n.745A=
XR_943452.1:n.691A=
NM_001320415.1:c.172A=	NP_001307344.1:p.Ser58=
XM_017021312.2:c.172A=	XP_016876801.1:p.Ser58=
XM_017021313.1:c.172A=	XP_016876802.1:p.Ser58=
XR_001750326.2:n.706A=
XR_001750327.2:n.625A=
XR_002957553.1:n.1139A=
XR_943450.3:n.729A=
XR_943451.3:n.745A=
XR_943452.3:n.690A=
NM_001320415.2:c.172A=	NP_001307344.1:p.Ser58=
NM_002382.5:c.361A= MANE Select	NP_002373.3:p.Ser121=
NM_145112.3:c.334A=	NP_660087.1:p.Ser112=
NM_145113.3:c.*150A=	NP_660088.1:n.*150A=
NM_001271069.2:c.144+17110A=	NP_001257998.1:n.144+17110A=
NM_197957.4:c.171+17110A=	NP_932061.1:n.171+17110A=