Canonical Allele Identifier: CA390030840

Gene: MAX

Linked Data

• MyVariant Identifiers: chr14:g.65543174G>T (hg19) ; chr14:g.65076456G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076456G>T , CM000676.2:g.65076456G>T	GRCh38
NC_000014.8:g.65543174G>T , CM000676.1:g.65543174G>T	GRCh37
NC_000014.7:g.64612927G>T	NCBI36
NG_029830.1:g.31054C>A , LRG_530:g.31054C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.*20C>A	ENSP00000452206.2:n.*20C>A
ENST00000556979.6:c.*956C>A	ENSP00000452378.1:n.*956C>A
ENST00000358664.9:c.*20C>A MANE Select	ENSP00000351490.4:n.*20C>A
ENST00000651648.1:c.145-6087C>A	ENSP00000498863.1:n.145-6087C>A
ENST00000284165.10:c.*1347C>A	ENSP00000284165.6:n.*1347C>A
ENST00000341653.6:c.171+17252C>A	ENSP00000342482.2:n.171+17252C>A
ENST00000358402.8:c.*20C>A	ENSP00000351175.4:n.*20C>A
ENST00000358664.8:c.*20C>A	ENSP00000351490.4:n.*20C>A
ENST00000394606.6:c.*276C>A	ENSP00000378104.2:n.*276C>A
ENST00000555419.5:c.395C>A	ENSP00000452405.1:n.395C>A
ENST00000555932.5:c.244C>A	ENSP00000450763.1:p.Gln82Lys
ENST00000618858.4:c.*292C>A	ENSP00000480127.1:n.*292C>A
NM_001271069.1:c.144+17252C>A	NP_001257998.1:n.144+17252C>A
NM_002382.4:c.*20C>A	NP_002373.3:n.*20C>A
NM_145112.2:c.*20C>A	NP_660087.1:n.*20C>A
NM_145113.2:c.*292C>A	NP_660088.1:n.*292C>A
NM_197957.3:c.171+17252C>A	NP_932061.1:n.171+17252C>A
NR_073137.1:n.627C>A
XR_429315.2:n.790C>A
NM_001320415.1:c.*20C>A	NP_001307344.1:n.*20C>A
XM_017021312.2:c.*20C>A	XP_016876801.1:n.*20C>A
XM_017021313.1:c.*20C>A	XP_016876802.1:n.*20C>A
XR_001750326.2:n.848C>A
XR_001750327.2:n.767C>A
XR_002957553.1:n.1281C>A
XR_943450.3:n.871C>A
XR_943451.3:n.887C>A
XR_943452.3:n.832C>A
NM_001320415.2:c.*20C>A	NP_001307344.1:n.*20C>A
NM_002382.5:c.*20C>A MANE Select	NP_002373.3:n.*20C>A
NM_145112.3:c.*20C>A	NP_660087.1:n.*20C>A
NM_145113.3:c.*292C>A	NP_660088.1:n.*292C>A
NM_001271069.2:c.144+17252C>A	NP_001257998.1:n.144+17252C>A
NM_197957.4:c.171+17252C>A	NP_932061.1:n.171+17252C>A