Canonical Allele Identifier: CA390031046

Gene: MAX

Linked Data

• MyVariant Identifiers: chr14:g.65543199T>G (hg19) ; chr14:g.65076481T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076481T>G , CM000676.2:g.65076481T>G	GRCh38
NC_000014.8:g.65543199T>G , CM000676.1:g.65543199T>G	GRCh37
NC_000014.7:g.64612952T>G	NCBI36
NG_029830.1:g.31029A>C , LRG_530:g.31029A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.259A>C	ENSP00000452206.2:p.Ser87Arg
ENST00000556979.6:c.*931A>C	ENSP00000452378.1:n.*931A>C
ENST00000358664.9:c.478A>C MANE Select	ENSP00000351490.4:p.Ser160Arg
ENST00000651648.1:c.145-6112A>C	ENSP00000498863.1:n.145-6112A>C
ENST00000284165.10:c.*1322A>C	ENSP00000284165.6:n.*1322A>C
ENST00000341653.6:c.171+17227A>C	ENSP00000342482.2:n.171+17227A>C
ENST00000358402.8:c.451A>C	ENSP00000351175.4:p.Ser151Arg
ENST00000358664.8:c.478A>C	ENSP00000351490.4:p.Ser160Arg
ENST00000394606.6:c.*251A>C	ENSP00000378104.2:n.*251A>C
ENST00000553928.5:c.*267A>C	ENSP00000451907.1:n.*267A>C
ENST00000555419.5:c.370A>C	ENSP00000452405.1:p.Ser124Arg
ENST00000555932.5:c.219A>C	ENSP00000450763.1:p.Pro73=
ENST00000557277.5:c.289A>C	ENSP00000450955.1:p.Ser97Arg
ENST00000618858.4:c.*267A>C	ENSP00000480127.1:n.*267A>C
NM_001271069.1:c.144+17227A>C	NP_001257998.1:n.144+17227A>C
NM_002382.4:c.478A>C	NP_002373.3:p.Ser160Arg
NM_145112.2:c.451A>C	NP_660087.1:p.Ser151Arg
NM_145113.2:c.*267A>C	NP_660088.1:n.*267A>C
NM_197957.3:c.171+17227A>C	NP_932061.1:n.171+17227A>C
NR_073137.1:n.602A>C
XR_429315.2:n.765A>C
NM_001320415.1:c.289A>C	NP_001307344.1:p.Ser97Arg
XM_017021312.2:c.289A>C	XP_016876801.1:p.Ser97Arg
XM_017021313.1:c.289A>C	XP_016876802.1:p.Ser97Arg
XR_001750326.2:n.823A>C
XR_001750327.2:n.742A>C
XR_002957553.1:n.1256A>C
XR_943450.3:n.846A>C
XR_943451.3:n.862A>C
XR_943452.3:n.807A>C
NM_001320415.2:c.289A>C	NP_001307344.1:p.Ser97Arg
NM_002382.5:c.478A>C MANE Select	NP_002373.3:p.Ser160Arg
NM_145112.3:c.451A>C	NP_660087.1:p.Ser151Arg
NM_145113.3:c.*267A>C	NP_660088.1:n.*267A>C
NM_001271069.2:c.144+17227A>C	NP_001257998.1:n.144+17227A>C
NM_197957.4:c.171+17227A>C	NP_932061.1:n.171+17227A>C