Canonical Allele Identifier: CA2142951148

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075536G= , CM000676.2:g.65075536G=	GRCh38
NC_000014.8:g.65542254G= , CM000676.1:g.65542254G=	GRCh37
NC_000014.7:g.64612007G=	NCBI36
NG_029830.1:g.31974C= , LRG_530:g.31974C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*1876C=	ENSP00000452378.1:n.*1876C=
ENST00000358664.9:c.*940C= MANE Select	ENSP00000351490.4:n.*940C=
ENST00000651648.1:c.145-5167C=	ENSP00000498863.1:n.145-5167C=
ENST00000284165.10:c.*2267C=	ENSP00000284165.6:n.*2267C=
ENST00000341653.6:c.171+18172C=	ENSP00000342482.2:n.171+18172C=
ENST00000358402.8:c.*940C=	ENSP00000351175.4:n.*940C=
ENST00000394606.6:c.*1196C=	ENSP00000378104.2:n.*1196C=
ENST00000555932.5:c.*915C=	ENSP00000450763.1:n.*915C=
ENST00000618858.4:c.*1212C=	ENSP00000480127.1:n.*1212C=
NM_001271069.1:c.144+18172C=	NP_001257998.1:n.144+18172C=
NM_002382.4:c.*940C=	NP_002373.3:n.*940C=
NM_145112.2:c.*940C=	NP_660087.1:n.*940C=
NM_145113.2:c.*1212C=	NP_660088.1:n.*1212C=
NM_197957.3:c.171+18172C=	NP_932061.1:n.171+18172C=
NR_073137.1:n.1547C=
XR_429315.2:n.1710C=
NM_001320415.1:c.*940C=	NP_001307344.1:n.*940C=
XM_017021312.2:c.*940C=	XP_016876801.1:n.*940C=
XM_017021313.1:c.*940C=	XP_016876802.1:n.*940C=
XR_001750326.2:n.1768C=
XR_001750327.2:n.1687C=
XR_002957553.1:n.2201C=
XR_943450.3:n.1791C=
XR_943451.3:n.1807C=
XR_943452.3:n.1752C=
NM_001320415.2:c.*940C=	NP_001307344.1:n.*940C=
NM_002382.5:c.*940C= MANE Select	NP_002373.3:n.*940C=
NM_145112.3:c.*940C=	NP_660087.1:n.*940C=
NM_145113.3:c.*1212C=	NP_660088.1:n.*1212C=
NM_001271069.2:c.144+18172C=	NP_001257998.1:n.144+18172C=
NM_197957.4:c.171+18172C=	NP_932061.1:n.171+18172C=