Canonical Allele Identifier: CA2142951413

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076083C= , CM000676.2:g.65076083C=	GRCh38
NC_000014.8:g.65542801C= , CM000676.1:g.65542801C=	GRCh37
NC_000014.7:g.64612554C=	NCBI36
NG_029830.1:g.31427G= , LRG_530:g.31427G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*393G=	ENSP00000452206.2:n.*393G=
ENST00000556979.6:c.*1329G=	ENSP00000452378.1:n.*1329G=
ENST00000358664.9:c.*393G= MANE Select	ENSP00000351490.4:n.*393G=
ENST00000651648.1:c.145-5714G=	ENSP00000498863.1:n.145-5714G=
ENST00000284165.10:c.*1720G=	ENSP00000284165.6:n.*1720G=
ENST00000341653.6:c.171+17625G=	ENSP00000342482.2:n.171+17625G=
ENST00000358402.8:c.*393G=	ENSP00000351175.4:n.*393G=
ENST00000358664.8:c.*393G=	ENSP00000351490.4:n.*393G=
ENST00000394606.6:c.*649G=	ENSP00000378104.2:n.*649G=
ENST00000555932.5:c.*368G=	ENSP00000450763.1:n.*368G=
ENST00000618858.4:c.*665G=	ENSP00000480127.1:n.*665G=
NM_001271069.1:c.144+17625G=	NP_001257998.1:n.144+17625G=
NM_002382.4:c.*393G=	NP_002373.3:n.*393G=
NM_145112.2:c.*393G=	NP_660087.1:n.*393G=
NM_145113.2:c.*665G=	NP_660088.1:n.*665G=
NM_197957.3:c.171+17625G=	NP_932061.1:n.171+17625G=
NR_073137.1:n.1000G=
XR_429315.2:n.1163G=
NM_001320415.1:c.*393G=	NP_001307344.1:n.*393G=
XM_017021312.2:c.*393G=	XP_016876801.1:n.*393G=
XM_017021313.1:c.*393G=	XP_016876802.1:n.*393G=
XR_001750326.2:n.1221G=
XR_001750327.2:n.1140G=
XR_002957553.1:n.1654G=
XR_943450.3:n.1244G=
XR_943451.3:n.1260G=
XR_943452.3:n.1205G=
NM_001320415.2:c.*393G=	NP_001307344.1:n.*393G=
NM_002382.5:c.*393G= MANE Select	NP_002373.3:n.*393G=
NM_145112.3:c.*393G=	NP_660087.1:n.*393G=
NM_145113.3:c.*665G=	NP_660088.1:n.*665G=
NM_001271069.2:c.144+17625G=	NP_001257998.1:n.144+17625G=
NM_197957.4:c.171+17625G=	NP_932061.1:n.171+17625G=