Canonical Allele Identifier: CA707762170

Gene: MAX

Linked Data

• dbSNP Id: rs1229228088
• MyVariant Identifiers: chr14:g.65569174C>G (hg19) ; chr14:g.65102456C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65102456C>G , CM000676.2:g.65102456C>G	GRCh38
NC_000014.8:g.65569174C>G , CM000676.1:g.65569174C>G	GRCh37
NC_000014.7:g.64638927C>G	NCBI36
NG_029830.1:g.5054G>C , LRG_530:g.5054G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.-157+53G>C	ENSP00000452206.2:n.-157+53G>C
ENST00000556979.6:c.-117G>C	ENSP00000452378.1:n.-117G>C
ENST00000358664.9:c.-117G>C MANE Select	ENSP00000351490.4:n.-117G>C
ENST00000246163.2:c.-117G>C	ENSP00000246163.2:n.-117G>C
ENST00000284165.10:c.-117G>C	ENSP00000284165.6:n.-117G>C
ENST00000358402.8:c.-117G>C	ENSP00000351175.4:n.-117G>C
ENST00000358664.8:c.-117G>C	ENSP00000351490.4:n.-117G>C
ENST00000394606.6:c.-117G>C	ENSP00000378104.2:n.-117G>C
ENST00000554709.1:n.62G>C
ENST00000555667.5:c.-117G>C	ENSP00000452286.1:n.-117G>C
ENST00000555932.5:c.-117G>C	ENSP00000450763.1:n.-117G>C
ENST00000556443.5:c.-117G>C	ENSP00000450818.1:n.-117G>C
ENST00000556702.1:n.23G>C
ENST00000556892.5:c.-157+53G>C	ENSP00000452206.1:n.-157+53G>C
ENST00000556979.5:c.-117G>C	ENSP00000452378.1:n.-117G>C
ENST00000557277.5:c.-239+53G>C	ENSP00000450955.1:n.-239+53G>C
ENST00000557746.5:c.-117G>C	ENSP00000452197.1:n.-117G>C
ENST00000618858.4:c.-117G>C	ENSP00000480127.1:n.-117G>C
NM_001271068.1:c.-117G>C	NP_001257997.1:n.-117G>C
NM_001271069.1:c.-117G>C	NP_001257998.1:n.-117G>C
NM_002382.4:c.-117G>C	NP_002373.3:n.-117G>C
NM_145112.2:c.-117G>C	NP_660087.1:n.-117G>C
NM_145113.2:c.-117G>C	NP_660088.1:n.-117G>C
NM_145114.2:c.-117G>C	NP_660089.1:n.-117G>C
NM_197957.3:c.-117G>C	NP_932061.1:n.-117G>C
NR_073137.1:n.187+53G>C
NR_073138.1:n.187+53G>C
XM_011536773.1:c.-117G>C	XP_011535075.1:n.-117G>C
XR_429315.2:n.86G>C
XR_943450.1:n.86G>C
XR_943451.1:n.86G>C
XR_943452.1:n.75G>C
NM_001320415.1:c.-391G>C	NP_001307344.1:n.-391G>C
XM_011536773.3:c.-117G>C	XP_011535075.1:n.-117G>C
XM_017021312.2:c.-364G>C	XP_016876801.1:n.-364G>C
XR_001750326.2:n.74G>C
XR_001750327.2:n.74G>C
XR_002957553.1:n.77G>C
XR_943450.3:n.86G>C
XR_943451.3:n.86G>C
XR_943452.3:n.74G>C
NM_001320415.2:c.-391G>C	NP_001307344.1:n.-391G>C
NM_002382.5:c.-117G>C MANE Select	NP_002373.3:n.-117G>C
NM_145112.3:c.-117G>C	NP_660087.1:n.-117G>C
NM_145113.3:c.-117G>C	NP_660088.1:n.-117G>C
NM_001271068.2:c.-117G>C	NP_001257997.1:n.-117G>C
NM_001271069.2:c.-117G>C	NP_001257998.1:n.-117G>C
NM_145114.3:c.-117G>C	NP_660089.1:n.-117G>C
NM_197957.4:c.-117G>C	NP_932061.1:n.-117G>C