Canonical Allele Identifier: CA2142951606

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076480C= , CM000676.2:g.65076480C=	GRCh38
NC_000014.8:g.65543198C= , CM000676.1:g.65543198C=	GRCh37
NC_000014.7:g.64612951C=	NCBI36
NG_029830.1:g.31030G= , LRG_530:g.31030G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.260G=	ENSP00000452206.2:p.Ser87=
ENST00000556979.6:c.*932G=	ENSP00000452378.1:n.*932G=
ENST00000358664.9:c.479G= MANE Select	ENSP00000351490.4:p.Ser160=
ENST00000651648.1:c.145-6111G=	ENSP00000498863.1:n.145-6111G=
ENST00000284165.10:c.*1323G=	ENSP00000284165.6:n.*1323G=
ENST00000341653.6:c.171+17228G=	ENSP00000342482.2:n.171+17228G=
ENST00000358402.8:c.452G=	ENSP00000351175.4:p.Ser151=
ENST00000358664.8:c.479G=	ENSP00000351490.4:p.Ser160=
ENST00000394606.6:c.*252G=	ENSP00000378104.2:n.*252G=
ENST00000553928.5:c.*268G=	ENSP00000451907.1:n.*268G=
ENST00000555419.5:c.371G=	ENSP00000452405.1:p.Ser124=
ENST00000555932.5:c.220G=	ENSP00000450763.1:p.Ala74=
ENST00000557277.5:c.290G=	ENSP00000450955.1:p.Ser97=
ENST00000618858.4:c.*268G=	ENSP00000480127.1:n.*268G=
NM_001271069.1:c.144+17228G=	NP_001257998.1:n.144+17228G=
NM_002382.4:c.479G=	NP_002373.3:p.Ser160=
NM_145112.2:c.452G=	NP_660087.1:p.Ser151=
NM_145113.2:c.*268G=	NP_660088.1:n.*268G=
NM_197957.3:c.171+17228G=	NP_932061.1:n.171+17228G=
NR_073137.1:n.603G=
XR_429315.2:n.766G=
NM_001320415.1:c.290G=	NP_001307344.1:p.Ser97=
XM_017021312.2:c.290G=	XP_016876801.1:p.Ser97=
XM_017021313.1:c.290G=	XP_016876802.1:p.Ser97=
XR_001750326.2:n.824G=
XR_001750327.2:n.743G=
XR_002957553.1:n.1257G=
XR_943450.3:n.847G=
XR_943451.3:n.863G=
XR_943452.3:n.808G=
NM_001320415.2:c.290G=	NP_001307344.1:p.Ser97=
NM_002382.5:c.479G= MANE Select	NP_002373.3:p.Ser160=
NM_145112.3:c.452G=	NP_660087.1:p.Ser151=
NM_145113.3:c.*268G=	NP_660088.1:n.*268G=
NM_001271069.2:c.144+17228G=	NP_001257998.1:n.144+17228G=
NM_197957.4:c.171+17228G=	NP_932061.1:n.171+17228G=