Canonical Allele Identifier: CA2142951228

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075705C= , CM000676.2:g.65075705C=	GRCh38
NC_000014.8:g.65542423C= , CM000676.1:g.65542423C=	GRCh37
NC_000014.7:g.64612176C=	NCBI36
NG_029830.1:g.31805G= , LRG_530:g.31805G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*771G=	ENSP00000452206.2:n.*771G=
ENST00000556979.6:c.*1707G=	ENSP00000452378.1:n.*1707G=
ENST00000358664.9:c.*771G= MANE Select	ENSP00000351490.4:n.*771G=
ENST00000651648.1:c.145-5336G=	ENSP00000498863.1:n.145-5336G=
ENST00000284165.10:c.*2098G=	ENSP00000284165.6:n.*2098G=
ENST00000341653.6:c.171+18003G=	ENSP00000342482.2:n.171+18003G=
ENST00000358402.8:c.*771G=	ENSP00000351175.4:n.*771G=
ENST00000358664.8:c.*771G=	ENSP00000351490.4:n.*771G=
ENST00000394606.6:c.*1027G=	ENSP00000378104.2:n.*1027G=
ENST00000555932.5:c.*746G=	ENSP00000450763.1:n.*746G=
ENST00000618858.4:c.*1043G=	ENSP00000480127.1:n.*1043G=
NM_001271069.1:c.144+18003G=	NP_001257998.1:n.144+18003G=
NM_002382.4:c.*771G=	NP_002373.3:n.*771G=
NM_145112.2:c.*771G=	NP_660087.1:n.*771G=
NM_145113.2:c.*1043G=	NP_660088.1:n.*1043G=
NM_197957.3:c.171+18003G=	NP_932061.1:n.171+18003G=
NR_073137.1:n.1378G=
XR_429315.2:n.1541G=
NM_001320415.1:c.*771G=	NP_001307344.1:n.*771G=
XM_017021312.2:c.*771G=	XP_016876801.1:n.*771G=
XM_017021313.1:c.*771G=	XP_016876802.1:n.*771G=
XR_001750326.2:n.1599G=
XR_001750327.2:n.1518G=
XR_002957553.1:n.2032G=
XR_943450.3:n.1622G=
XR_943451.3:n.1638G=
XR_943452.3:n.1583G=
NM_001320415.2:c.*771G=	NP_001307344.1:n.*771G=
NM_002382.5:c.*771G= MANE Select	NP_002373.3:n.*771G=
NM_145112.3:c.*771G=	NP_660087.1:n.*771G=
NM_145113.3:c.*1043G=	NP_660088.1:n.*1043G=
NM_001271069.2:c.144+18003G=	NP_001257998.1:n.144+18003G=
NM_197957.4:c.171+18003G=	NP_932061.1:n.171+18003G=