Canonical Allele Identifier: CA2142951113

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65075450C= , CM000676.2:g.65075450C=	GRCh38
NC_000014.8:g.65542168C= , CM000676.1:g.65542168C=	GRCh37
NC_000014.7:g.64611921C=	NCBI36
NG_029830.1:g.32060G= , LRG_530:g.32060G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556979.6:c.*1962G=	ENSP00000452378.1:n.*1962G=
ENST00000358664.9:c.*1026G= MANE Select	ENSP00000351490.4:n.*1026G=
ENST00000651648.1:c.145-5081G=	ENSP00000498863.1:n.145-5081G=
ENST00000284165.10:c.*2353G=	ENSP00000284165.6:n.*2353G=
ENST00000341653.6:c.171+18258G=	ENSP00000342482.2:n.171+18258G=
ENST00000358402.8:c.*1026G=	ENSP00000351175.4:n.*1026G=
ENST00000394606.6:c.*1282G=	ENSP00000378104.2:n.*1282G=
ENST00000555932.5:c.*1001G=	ENSP00000450763.1:n.*1001G=
ENST00000618858.4:c.*1298G=	ENSP00000480127.1:n.*1298G=
NM_001271069.1:c.144+18258G=	NP_001257998.1:n.144+18258G=
NM_002382.4:c.*1026G=	NP_002373.3:n.*1026G=
NM_145112.2:c.*1026G=	NP_660087.1:n.*1026G=
NM_145113.2:c.*1298G=	NP_660088.1:n.*1298G=
NM_197957.3:c.171+18258G=	NP_932061.1:n.171+18258G=
NR_073137.1:n.1633G=
XR_429315.2:n.1796G=
NM_001320415.1:c.*1026G=	NP_001307344.1:n.*1026G=
XM_017021312.2:c.*1026G=	XP_016876801.1:n.*1026G=
XM_017021313.1:c.*1026G=	XP_016876802.1:n.*1026G=
XR_001750326.2:n.1854G=
XR_001750327.2:n.1773G=
XR_002957553.1:n.2287G=
XR_943450.3:n.1877G=
XR_943451.3:n.1893G=
XR_943452.3:n.1838G=
NM_001320415.2:c.*1026G=	NP_001307344.1:n.*1026G=
NM_002382.5:c.*1026G= MANE Select	NP_002373.3:n.*1026G=
NM_145112.3:c.*1026G=	NP_660087.1:n.*1026G=
NM_145113.3:c.*1298G=	NP_660088.1:n.*1298G=
NM_001271069.2:c.144+18258G=	NP_001257998.1:n.144+18258G=
NM_197957.4:c.171+18258G=	NP_932061.1:n.171+18258G=