Canonical Allele Identifier: CA2142951127

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075486G= , CM000676.2:g.65075486G=	GRCh38
NC_000014.8:g.65542204G= , CM000676.1:g.65542204G=	GRCh37
NC_000014.7:g.64611957G=	NCBI36
NG_029830.1:g.32024C= , LRG_530:g.32024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*1926C=	ENSP00000452378.1:n.*1926C=
ENST00000358664.9:c.*990C= MANE Select	ENSP00000351490.4:n.*990C=
ENST00000651648.1:c.145-5117C=	ENSP00000498863.1:n.145-5117C=
ENST00000284165.10:c.*2317C=	ENSP00000284165.6:n.*2317C=
ENST00000341653.6:c.171+18222C=	ENSP00000342482.2:n.171+18222C=
ENST00000358402.8:c.*990C=	ENSP00000351175.4:n.*990C=
ENST00000394606.6:c.*1246C=	ENSP00000378104.2:n.*1246C=
ENST00000555932.5:c.*965C=	ENSP00000450763.1:n.*965C=
ENST00000618858.4:c.*1262C=	ENSP00000480127.1:n.*1262C=
NM_001271069.1:c.144+18222C=	NP_001257998.1:n.144+18222C=
NM_002382.4:c.*990C=	NP_002373.3:n.*990C=
NM_145112.2:c.*990C=	NP_660087.1:n.*990C=
NM_145113.2:c.*1262C=	NP_660088.1:n.*1262C=
NM_197957.3:c.171+18222C=	NP_932061.1:n.171+18222C=
NR_073137.1:n.1597C=
XR_429315.2:n.1760C=
NM_001320415.1:c.*990C=	NP_001307344.1:n.*990C=
XM_017021312.2:c.*990C=	XP_016876801.1:n.*990C=
XM_017021313.1:c.*990C=	XP_016876802.1:n.*990C=
XR_001750326.2:n.1818C=
XR_001750327.2:n.1737C=
XR_002957553.1:n.2251C=
XR_943450.3:n.1841C=
XR_943451.3:n.1857C=
XR_943452.3:n.1802C=
NM_001320415.2:c.*990C=	NP_001307344.1:n.*990C=
NM_002382.5:c.*990C= MANE Select	NP_002373.3:n.*990C=
NM_145112.3:c.*990C=	NP_660087.1:n.*990C=
NM_145113.3:c.*1262C=	NP_660088.1:n.*1262C=
NM_001271069.2:c.144+18222C=	NP_001257998.1:n.144+18222C=
NM_197957.4:c.171+18222C=	NP_932061.1:n.171+18222C=