Canonical Allele Identifier: CA2142951625

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076528G= , CM000676.2:g.65076528G=	GRCh38
NC_000014.8:g.65543246G= , CM000676.1:g.65543246G=	GRCh37
NC_000014.7:g.64612999G=	NCBI36
NG_029830.1:g.30982C= , LRG_530:g.30982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.212C=	ENSP00000452206.2:p.Ser71=
ENST00000556979.6:c.*884C=	ENSP00000452378.1:n.*884C=
ENST00000358664.9:c.431C= MANE Select	ENSP00000351490.4:p.Ser144=
ENST00000651648.1:c.145-6159C=	ENSP00000498863.1:n.145-6159C=
ENST00000284165.10:c.*1275C=	ENSP00000284165.6:n.*1275C=
ENST00000341653.6:c.171+17180C=	ENSP00000342482.2:n.171+17180C=
ENST00000358402.8:c.404C=	ENSP00000351175.4:p.Ser135=
ENST00000358664.8:c.431C=	ENSP00000351490.4:p.Ser144=
ENST00000394606.6:c.*204C=	ENSP00000378104.2:n.*204C=
ENST00000553928.5:c.*220C=	ENSP00000451907.1:n.*220C=
ENST00000555419.5:c.323C=	ENSP00000452405.1:p.Ser108=
ENST00000555932.5:c.172C=	ENSP00000450763.1:p.Leu58=
ENST00000557277.5:c.242C=	ENSP00000450955.1:p.Ser81=
ENST00000618858.4:c.*220C=	ENSP00000480127.1:n.*220C=
NM_001271069.1:c.144+17180C=	NP_001257998.1:n.144+17180C=
NM_002382.4:c.431C=	NP_002373.3:p.Ser144=
NM_145112.2:c.404C=	NP_660087.1:p.Ser135=
NM_145113.2:c.*220C=	NP_660088.1:n.*220C=
NM_197957.3:c.171+17180C=	NP_932061.1:n.171+17180C=
NR_073137.1:n.555C=
XR_429315.2:n.718C=
NM_001320415.1:c.242C=	NP_001307344.1:p.Ser81=
XM_017021312.2:c.242C=	XP_016876801.1:p.Ser81=
XM_017021313.1:c.242C=	XP_016876802.1:p.Ser81=
XR_001750326.2:n.776C=
XR_001750327.2:n.695C=
XR_002957553.1:n.1209C=
XR_943450.3:n.799C=
XR_943451.3:n.815C=
XR_943452.3:n.760C=
NM_001320415.2:c.242C=	NP_001307344.1:p.Ser81=
NM_002382.5:c.431C= MANE Select	NP_002373.3:p.Ser144=
NM_145112.3:c.404C=	NP_660087.1:p.Ser135=
NM_145113.3:c.*220C=	NP_660088.1:n.*220C=
NM_001271069.2:c.144+17180C=	NP_001257998.1:n.144+17180C=
NM_197957.4:c.171+17180C=	NP_932061.1:n.171+17180C=