Canonical Allele Identifier: CA390031345

Gene: MAX

Linked Data

• MyVariant Identifiers: chr14:g.65543242C>G (hg19) ; chr14:g.65076524C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076524C>G , CM000676.2:g.65076524C>G	GRCh38
NC_000014.8:g.65543242C>G , CM000676.1:g.65543242C>G	GRCh37
NC_000014.7:g.64612995C>G	NCBI36
NG_029830.1:g.30986G>C , LRG_530:g.30986G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.216G>C	ENSP00000452206.2:p.Glu72Asp
ENST00000556979.6:c.*888G>C	ENSP00000452378.1:n.*888G>C
ENST00000358664.9:c.435G>C MANE Select	ENSP00000351490.4:p.Glu145Asp
ENST00000651648.1:c.145-6155G>C	ENSP00000498863.1:n.145-6155G>C
ENST00000284165.10:c.*1279G>C	ENSP00000284165.6:n.*1279G>C
ENST00000341653.6:c.171+17184G>C	ENSP00000342482.2:n.171+17184G>C
ENST00000358402.8:c.408G>C	ENSP00000351175.4:p.Glu136Asp
ENST00000358664.8:c.435G>C	ENSP00000351490.4:p.Glu145Asp
ENST00000394606.6:c.*208G>C	ENSP00000378104.2:n.*208G>C
ENST00000553928.5:c.*224G>C	ENSP00000451907.1:n.*224G>C
ENST00000555419.5:c.327G>C	ENSP00000452405.1:p.Glu109Asp
ENST00000555932.5:c.176G>C	ENSP00000450763.1:p.Ser59Thr
ENST00000557277.5:c.246G>C	ENSP00000450955.1:p.Glu82Asp
ENST00000618858.4:c.*224G>C	ENSP00000480127.1:n.*224G>C
NM_001271069.1:c.144+17184G>C	NP_001257998.1:n.144+17184G>C
NM_002382.4:c.435G>C	NP_002373.3:p.Glu145Asp
NM_145112.2:c.408G>C	NP_660087.1:p.Glu136Asp
NM_145113.2:c.*224G>C	NP_660088.1:n.*224G>C
NM_197957.3:c.171+17184G>C	NP_932061.1:n.171+17184G>C
NR_073137.1:n.559G>C
XR_429315.2:n.722G>C
NM_001320415.1:c.246G>C	NP_001307344.1:p.Glu82Asp
XM_017021312.2:c.246G>C	XP_016876801.1:p.Glu82Asp
XM_017021313.1:c.246G>C	XP_016876802.1:p.Glu82Asp
XR_001750326.2:n.780G>C
XR_001750327.2:n.699G>C
XR_002957553.1:n.1213G>C
XR_943450.3:n.803G>C
XR_943451.3:n.819G>C
XR_943452.3:n.764G>C
NM_001320415.2:c.246G>C	NP_001307344.1:p.Glu82Asp
NM_002382.5:c.435G>C MANE Select	NP_002373.3:p.Glu145Asp
NM_145112.3:c.408G>C	NP_660087.1:p.Glu136Asp
NM_145113.3:c.*224G>C	NP_660088.1:n.*224G>C
NM_001271069.2:c.144+17184G>C	NP_001257998.1:n.144+17184G>C
NM_197957.4:c.171+17184G>C	NP_932061.1:n.171+17184G>C