Canonical Allele Identifier: CA2142951094

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075411T= , CM000676.2:g.65075411T=	GRCh38
NC_000014.8:g.65542129T= , CM000676.1:g.65542129T=	GRCh37
NC_000014.7:g.64611882T=	NCBI36
NG_029830.1:g.32099A= , LRG_530:g.32099A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*2001A=	ENSP00000452378.1:n.*2001A=
ENST00000358664.9:c.*1065A= MANE Select	ENSP00000351490.4:n.*1065A=
ENST00000651648.1:c.145-5042A=	ENSP00000498863.1:n.145-5042A=
ENST00000284165.10:c.*2392A=	ENSP00000284165.6:n.*2392A=
ENST00000341653.6:c.171+18297A=	ENSP00000342482.2:n.171+18297A=
ENST00000358402.8:c.*1065A=	ENSP00000351175.4:n.*1065A=
ENST00000394606.6:c.*1321A=	ENSP00000378104.2:n.*1321A=
ENST00000555932.5:c.*1040A=	ENSP00000450763.1:n.*1040A=
ENST00000618858.4:c.*1337A=	ENSP00000480127.1:n.*1337A=
NM_001271069.1:c.144+18297A=	NP_001257998.1:n.144+18297A=
NM_002382.4:c.*1065A=	NP_002373.3:n.*1065A=
NM_145112.2:c.*1065A=	NP_660087.1:n.*1065A=
NM_145113.2:c.*1337A=	NP_660088.1:n.*1337A=
NM_197957.3:c.171+18297A=	NP_932061.1:n.171+18297A=
NR_073137.1:n.1672A=
XR_429315.2:n.1835A=
NM_001320415.1:c.*1065A=	NP_001307344.1:n.*1065A=
XM_017021312.2:c.*1065A=	XP_016876801.1:n.*1065A=
XM_017021313.1:c.*1065A=	XP_016876802.1:n.*1065A=
XR_001750326.2:n.1893A=
XR_001750327.2:n.1812A=
XR_002957553.1:n.2326A=
XR_943450.3:n.1916A=
XR_943451.3:n.1932A=
XR_943452.3:n.1877A=
NM_001320415.2:c.*1065A=	NP_001307344.1:n.*1065A=
NM_002382.5:c.*1065A= MANE Select	NP_002373.3:n.*1065A=
NM_145112.3:c.*1065A=	NP_660087.1:n.*1065A=
NM_145113.3:c.*1337A=	NP_660088.1:n.*1337A=
NM_001271069.2:c.144+18297A=	NP_001257998.1:n.144+18297A=
NM_197957.4:c.171+18297A=	NP_932061.1:n.171+18297A=