Canonical Allele Identifier: CA2142951387

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076033G= , CM000676.2:g.65076033G=	GRCh38
NC_000014.8:g.65542751G= , CM000676.1:g.65542751G=	GRCh37
NC_000014.7:g.64612504G=	NCBI36
NG_029830.1:g.31477C= , LRG_530:g.31477C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*443C=	ENSP00000452206.2:n.*443C=
ENST00000556979.6:c.*1379C=	ENSP00000452378.1:n.*1379C=
ENST00000358664.9:c.*443C= MANE Select	ENSP00000351490.4:n.*443C=
ENST00000651648.1:c.145-5664C=	ENSP00000498863.1:n.145-5664C=
ENST00000284165.10:c.*1770C=	ENSP00000284165.6:n.*1770C=
ENST00000341653.6:c.171+17675C=	ENSP00000342482.2:n.171+17675C=
ENST00000358402.8:c.*443C=	ENSP00000351175.4:n.*443C=
ENST00000358664.8:c.*443C=	ENSP00000351490.4:n.*443C=
ENST00000394606.6:c.*699C=	ENSP00000378104.2:n.*699C=
ENST00000555932.5:c.*418C=	ENSP00000450763.1:n.*418C=
ENST00000618858.4:c.*715C=	ENSP00000480127.1:n.*715C=
NM_001271069.1:c.144+17675C=	NP_001257998.1:n.144+17675C=
NM_002382.4:c.*443C=	NP_002373.3:n.*443C=
NM_145112.2:c.*443C=	NP_660087.1:n.*443C=
NM_145113.2:c.*715C=	NP_660088.1:n.*715C=
NM_197957.3:c.171+17675C=	NP_932061.1:n.171+17675C=
NR_073137.1:n.1050C=
XR_429315.2:n.1213C=
NM_001320415.1:c.*443C=	NP_001307344.1:n.*443C=
XM_017021312.2:c.*443C=	XP_016876801.1:n.*443C=
XM_017021313.1:c.*443C=	XP_016876802.1:n.*443C=
XR_001750326.2:n.1271C=
XR_001750327.2:n.1190C=
XR_002957553.1:n.1704C=
XR_943450.3:n.1294C=
XR_943451.3:n.1310C=
XR_943452.3:n.1255C=
NM_001320415.2:c.*443C=	NP_001307344.1:n.*443C=
NM_002382.5:c.*443C= MANE Select	NP_002373.3:n.*443C=
NM_145112.3:c.*443C=	NP_660087.1:n.*443C=
NM_145113.3:c.*715C=	NP_660088.1:n.*715C=
NM_001271069.2:c.144+17675C=	NP_001257998.1:n.144+17675C=
NM_197957.4:c.171+17675C=	NP_932061.1:n.171+17675C=