Canonical Allele Identifier: CA2142951400

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076064G= , CM000676.2:g.65076064G=	GRCh38
NC_000014.8:g.65542782G= , CM000676.1:g.65542782G=	GRCh37
NC_000014.7:g.64612535G=	NCBI36
NG_029830.1:g.31446C= , LRG_530:g.31446C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*412C=	ENSP00000452206.2:n.*412C=
ENST00000556979.6:c.*1348C=	ENSP00000452378.1:n.*1348C=
ENST00000358664.9:c.*412C= MANE Select	ENSP00000351490.4:n.*412C=
ENST00000651648.1:c.145-5695C=	ENSP00000498863.1:n.145-5695C=
ENST00000284165.10:c.*1739C=	ENSP00000284165.6:n.*1739C=
ENST00000341653.6:c.171+17644C=	ENSP00000342482.2:n.171+17644C=
ENST00000358402.8:c.*412C=	ENSP00000351175.4:n.*412C=
ENST00000358664.8:c.*412C=	ENSP00000351490.4:n.*412C=
ENST00000394606.6:c.*668C=	ENSP00000378104.2:n.*668C=
ENST00000555932.5:c.*387C=	ENSP00000450763.1:n.*387C=
ENST00000618858.4:c.*684C=	ENSP00000480127.1:n.*684C=
NM_001271069.1:c.144+17644C=	NP_001257998.1:n.144+17644C=
NM_002382.4:c.*412C=	NP_002373.3:n.*412C=
NM_145112.2:c.*412C=	NP_660087.1:n.*412C=
NM_145113.2:c.*684C=	NP_660088.1:n.*684C=
NM_197957.3:c.171+17644C=	NP_932061.1:n.171+17644C=
NR_073137.1:n.1019C=
XR_429315.2:n.1182C=
NM_001320415.1:c.*412C=	NP_001307344.1:n.*412C=
XM_017021312.2:c.*412C=	XP_016876801.1:n.*412C=
XM_017021313.1:c.*412C=	XP_016876802.1:n.*412C=
XR_001750326.2:n.1240C=
XR_001750327.2:n.1159C=
XR_002957553.1:n.1673C=
XR_943450.3:n.1263C=
XR_943451.3:n.1279C=
XR_943452.3:n.1224C=
NM_001320415.2:c.*412C=	NP_001307344.1:n.*412C=
NM_002382.5:c.*412C= MANE Select	NP_002373.3:n.*412C=
NM_145112.3:c.*412C=	NP_660087.1:n.*412C=
NM_145113.3:c.*684C=	NP_660088.1:n.*684C=
NM_001271069.2:c.144+17644C=	NP_001257998.1:n.144+17644C=
NM_197957.4:c.171+17644C=	NP_932061.1:n.171+17644C=