Canonical Allele Identifier: CA2142951445

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076152G= , CM000676.2:g.65076152G=	GRCh38
NC_000014.8:g.65542870G= , CM000676.1:g.65542870G=	GRCh37
NC_000014.7:g.64612623G=	NCBI36
NG_029830.1:g.31358C= , LRG_530:g.31358C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*324C=	ENSP00000452206.2:n.*324C=
ENST00000556979.6:c.*1260C=	ENSP00000452378.1:n.*1260C=
ENST00000358664.9:c.*324C= MANE Select	ENSP00000351490.4:n.*324C=
ENST00000651648.1:c.145-5783C=	ENSP00000498863.1:n.145-5783C=
ENST00000284165.10:c.*1651C=	ENSP00000284165.6:n.*1651C=
ENST00000341653.6:c.171+17556C=	ENSP00000342482.2:n.171+17556C=
ENST00000358402.8:c.*324C=	ENSP00000351175.4:n.*324C=
ENST00000358664.8:c.*324C=	ENSP00000351490.4:n.*324C=
ENST00000394606.6:c.*580C=	ENSP00000378104.2:n.*580C=
ENST00000555419.5:c.699C=	ENSP00000452405.1:n.699C=
ENST00000555932.5:c.*299C=	ENSP00000450763.1:n.*299C=
ENST00000618858.4:c.*596C=	ENSP00000480127.1:n.*596C=
NM_001271069.1:c.144+17556C=	NP_001257998.1:n.144+17556C=
NM_002382.4:c.*324C=	NP_002373.3:n.*324C=
NM_145112.2:c.*324C=	NP_660087.1:n.*324C=
NM_145113.2:c.*596C=	NP_660088.1:n.*596C=
NM_197957.3:c.171+17556C=	NP_932061.1:n.171+17556C=
NR_073137.1:n.931C=
XR_429315.2:n.1094C=
NM_001320415.1:c.*324C=	NP_001307344.1:n.*324C=
XM_017021312.2:c.*324C=	XP_016876801.1:n.*324C=
XM_017021313.1:c.*324C=	XP_016876802.1:n.*324C=
XR_001750326.2:n.1152C=
XR_001750327.2:n.1071C=
XR_002957553.1:n.1585C=
XR_943450.3:n.1175C=
XR_943451.3:n.1191C=
XR_943452.3:n.1136C=
NM_001320415.2:c.*324C=	NP_001307344.1:n.*324C=
NM_002382.5:c.*324C= MANE Select	NP_002373.3:n.*324C=
NM_145112.3:c.*324C=	NP_660087.1:n.*324C=
NM_145113.3:c.*596C=	NP_660088.1:n.*596C=
NM_001271069.2:c.144+17556C=	NP_001257998.1:n.144+17556C=
NM_197957.4:c.171+17556C=	NP_932061.1:n.171+17556C=