Canonical Allele Identifier: CA7232793

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076549C>T , CM000676.2:g.65076549C>T	GRCh38
NC_000014.8:g.65543267C>T , CM000676.1:g.65543267C>T	GRCh37
NC_000014.7:g.64613020C>T	NCBI36
NG_029830.1:g.30961G>A , LRG_530:g.30961G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002382.5:c.410G>A MANE Select	NP_002373.3:p.Gly137Asp
ENST00000358664.9:c.410G>A MANE Select	ENSP00000351490.4:p.Gly137Asp
NM_001271069.1:c.144+17159G>A	NP_001257998.1:n.144+17159G>A
NM_001271069.2:c.144+17159G>A	NP_001257998.1:n.144+17159G>A
NM_001320415.1:c.221G>A	NP_001307344.1:p.Gly74Asp
NM_001320415.2:c.221G>A	NP_001307344.1:p.Gly74Asp
NM_002382.4:c.410G>A	NP_002373.3:p.Gly137Asp
NM_145112.2:c.383G>A	NP_660087.1:p.Gly128Asp
NM_145112.3:c.383G>A	NP_660087.1:p.Gly128Asp
NM_145113.2:c.*199G>A	NP_660088.1:n.*199G>A
NM_145113.3:c.*199G>A	NP_660088.1:n.*199G>A
NM_197957.3:c.171+17159G>A	NP_932061.1:n.171+17159G>A
NM_197957.4:c.171+17159G>A	NP_932061.1:n.171+17159G>A
NR_073137.1:n.534G>A
ENST00000284165.10:c.*1254G>A	ENSP00000284165.6:n.*1254G>A
ENST00000341653.6:c.171+17159G>A	ENSP00000342482.2:n.171+17159G>A
ENST00000358402.8:c.383G>A	ENSP00000351175.4:p.Gly128Asp
ENST00000358664.8:c.410G>A	ENSP00000351490.4:p.Gly137Asp
ENST00000394606.6:c.*183G>A	ENSP00000378104.2:n.*183G>A
ENST00000553928.5:c.*199G>A	ENSP00000451907.1:n.*199G>A
ENST00000555419.5:c.302G>A	ENSP00000452405.1:p.Gly101Asp
ENST00000555932.5:c.151G>A	ENSP00000450763.1:p.Ala51Thr
ENST00000556892.6:c.191G>A	ENSP00000452206.2:p.Gly64Asp
ENST00000556979.6:c.*863G>A	ENSP00000452378.1:n.*863G>A
ENST00000557277.5:c.221G>A	ENSP00000450955.1:p.Gly74Asp
ENST00000618858.4:c.*199G>A	ENSP00000480127.1:n.*199G>A
ENST00000651648.1:c.145-6180G>A	ENSP00000498863.1:n.145-6180G>A
XM_017021312.2:c.221G>A	XP_016876801.1:p.Gly74Asp
XM_017021313.1:c.221G>A	XP_016876802.1:p.Gly74Asp
XR_001750326.2:n.755G>A
XR_001750327.2:n.674G>A
XR_002957553.1:n.1188G>A
XR_429315.2:n.697G>A
XR_943450.3:n.778G>A
XR_943451.3:n.794G>A
XR_943452.3:n.739G>A