Canonical Allele Identifier: CA2142951112

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075449A= , CM000676.2:g.65075449A=	GRCh38
NC_000014.8:g.65542167A= , CM000676.1:g.65542167A=	GRCh37
NC_000014.7:g.64611920A=	NCBI36
NG_029830.1:g.32061T= , LRG_530:g.32061T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*1963T=	ENSP00000452378.1:n.*1963T=
ENST00000358664.9:c.*1027T= MANE Select	ENSP00000351490.4:n.*1027T=
ENST00000651648.1:c.145-5080T=	ENSP00000498863.1:n.145-5080T=
ENST00000284165.10:c.*2354T=	ENSP00000284165.6:n.*2354T=
ENST00000341653.6:c.171+18259T=	ENSP00000342482.2:n.171+18259T=
ENST00000358402.8:c.*1027T=	ENSP00000351175.4:n.*1027T=
ENST00000394606.6:c.*1283T=	ENSP00000378104.2:n.*1283T=
ENST00000555932.5:c.*1002T=	ENSP00000450763.1:n.*1002T=
ENST00000618858.4:c.*1299T=	ENSP00000480127.1:n.*1299T=
NM_001271069.1:c.144+18259T=	NP_001257998.1:n.144+18259T=
NM_002382.4:c.*1027T=	NP_002373.3:n.*1027T=
NM_145112.2:c.*1027T=	NP_660087.1:n.*1027T=
NM_145113.2:c.*1299T=	NP_660088.1:n.*1299T=
NM_197957.3:c.171+18259T=	NP_932061.1:n.171+18259T=
NR_073137.1:n.1634T=
XR_429315.2:n.1797T=
NM_001320415.1:c.*1027T=	NP_001307344.1:n.*1027T=
XM_017021312.2:c.*1027T=	XP_016876801.1:n.*1027T=
XM_017021313.1:c.*1027T=	XP_016876802.1:n.*1027T=
XR_001750326.2:n.1855T=
XR_001750327.2:n.1774T=
XR_002957553.1:n.2288T=
XR_943450.3:n.1878T=
XR_943451.3:n.1894T=
XR_943452.3:n.1839T=
NM_001320415.2:c.*1027T=	NP_001307344.1:n.*1027T=
NM_002382.5:c.*1027T= MANE Select	NP_002373.3:n.*1027T=
NM_145112.3:c.*1027T=	NP_660087.1:n.*1027T=
NM_145113.3:c.*1299T=	NP_660088.1:n.*1299T=
NM_001271069.2:c.144+18259T=	NP_001257998.1:n.144+18259T=
NM_197957.4:c.171+18259T=	NP_932061.1:n.171+18259T=