Canonical Allele Identifier: CA2142951648

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076579T= , CM000676.2:g.65076579T=	GRCh38
NC_000014.8:g.65543297T= , CM000676.1:g.65543297T=	GRCh37
NC_000014.7:g.64613050T=	NCBI36
NG_029830.1:g.30931A= , LRG_530:g.30931A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.161A=	ENSP00000452206.2:p.Lys54=
ENST00000556979.6:c.*833A=	ENSP00000452378.1:n.*833A=
ENST00000358664.9:c.380A= MANE Select	ENSP00000351490.4:p.Lys127=
ENST00000651648.1:c.145-6210A=	ENSP00000498863.1:n.145-6210A=
ENST00000284165.10:c.*1224A=	ENSP00000284165.6:n.*1224A=
ENST00000341653.6:c.171+17129A=	ENSP00000342482.2:n.171+17129A=
ENST00000358402.8:c.353A=	ENSP00000351175.4:p.Lys118=
ENST00000358664.8:c.380A=	ENSP00000351490.4:p.Lys127=
ENST00000394606.6:c.*153A=	ENSP00000378104.2:n.*153A=
ENST00000553928.5:c.*169A=	ENSP00000451907.1:n.*169A=
ENST00000555419.5:c.272A=	ENSP00000452405.1:p.Lys91=
ENST00000555932.5:c.121A=	ENSP00000450763.1:p.Arg41=
ENST00000557277.5:c.191A=	ENSP00000450955.1:p.Lys64=
ENST00000618858.4:c.*169A=	ENSP00000480127.1:n.*169A=
NM_001271069.1:c.144+17129A=	NP_001257998.1:n.144+17129A=
NM_002382.4:c.380A=	NP_002373.3:p.Lys127=
NM_145112.2:c.353A=	NP_660087.1:p.Lys118=
NM_145113.2:c.*169A=	NP_660088.1:n.*169A=
NM_197957.3:c.171+17129A=	NP_932061.1:n.171+17129A=
NR_073137.1:n.504A=
XR_429315.2:n.667A=
XR_943450.1:n.748A=
XR_943451.1:n.764A=
XR_943452.1:n.710A=
NM_001320415.1:c.191A=	NP_001307344.1:p.Lys64=
XM_017021312.2:c.191A=	XP_016876801.1:p.Lys64=
XM_017021313.1:c.191A=	XP_016876802.1:p.Lys64=
XR_001750326.2:n.725A=
XR_001750327.2:n.644A=
XR_002957553.1:n.1158A=
XR_943450.3:n.748A=
XR_943451.3:n.764A=
XR_943452.3:n.709A=
NM_001320415.2:c.191A=	NP_001307344.1:p.Lys64=
NM_002382.5:c.380A= MANE Select	NP_002373.3:p.Lys127=
NM_145112.3:c.353A=	NP_660087.1:p.Lys118=
NM_145113.3:c.*169A=	NP_660088.1:n.*169A=
NM_001271069.2:c.144+17129A=	NP_001257998.1:n.144+17129A=
NM_197957.4:c.171+17129A=	NP_932061.1:n.171+17129A=