Canonical Allele Identifier: CA2142951349

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075942C= , CM000676.2:g.65075942C=	GRCh38
NC_000014.8:g.65542660C= , CM000676.1:g.65542660C=	GRCh37
NC_000014.7:g.64612413C=	NCBI36
NG_029830.1:g.31568G= , LRG_530:g.31568G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*534G=	ENSP00000452206.2:n.*534G=
ENST00000556979.6:c.*1470G=	ENSP00000452378.1:n.*1470G=
ENST00000358664.9:c.*534G= MANE Select	ENSP00000351490.4:n.*534G=
ENST00000651648.1:c.145-5573G=	ENSP00000498863.1:n.145-5573G=
ENST00000284165.10:c.*1861G=	ENSP00000284165.6:n.*1861G=
ENST00000341653.6:c.171+17766G=	ENSP00000342482.2:n.171+17766G=
ENST00000358402.8:c.*534G=	ENSP00000351175.4:n.*534G=
ENST00000358664.8:c.*534G=	ENSP00000351490.4:n.*534G=
ENST00000394606.6:c.*790G=	ENSP00000378104.2:n.*790G=
ENST00000555932.5:c.*509G=	ENSP00000450763.1:n.*509G=
ENST00000618858.4:c.*806G=	ENSP00000480127.1:n.*806G=
NM_001271069.1:c.144+17766G=	NP_001257998.1:n.144+17766G=
NM_002382.4:c.*534G=	NP_002373.3:n.*534G=
NM_145112.2:c.*534G=	NP_660087.1:n.*534G=
NM_145113.2:c.*806G=	NP_660088.1:n.*806G=
NM_197957.3:c.171+17766G=	NP_932061.1:n.171+17766G=
NR_073137.1:n.1141G=
XR_429315.2:n.1304G=
NM_001320415.1:c.*534G=	NP_001307344.1:n.*534G=
XM_017021312.2:c.*534G=	XP_016876801.1:n.*534G=
XM_017021313.1:c.*534G=	XP_016876802.1:n.*534G=
XR_001750326.2:n.1362G=
XR_001750327.2:n.1281G=
XR_002957553.1:n.1795G=
XR_943450.3:n.1385G=
XR_943451.3:n.1401G=
XR_943452.3:n.1346G=
NM_001320415.2:c.*534G=	NP_001307344.1:n.*534G=
NM_002382.5:c.*534G= MANE Select	NP_002373.3:n.*534G=
NM_145112.3:c.*534G=	NP_660087.1:n.*534G=
NM_145113.3:c.*806G=	NP_660088.1:n.*806G=
NM_001271069.2:c.144+17766G=	NP_001257998.1:n.144+17766G=
NM_197957.4:c.171+17766G=	NP_932061.1:n.171+17766G=