Canonical Allele Identifier: CA390031753

Gene: MAX

Linked Data

• ClinVar Variation Id: 882142
• ClinVar RCV Id: RCV001111566
• dbSNP Id: rs2063062933
• MyVariant Identifiers: chr14:g.65543304T>G (hg19) ; chr14:g.65076586T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076586T>G , CM000676.2:g.65076586T>G	GRCh38
NC_000014.8:g.65543304T>G , CM000676.1:g.65543304T>G	GRCh37
NC_000014.7:g.64613057T>G	NCBI36
NG_029830.1:g.30924A>C , LRG_530:g.30924A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.154A>C	ENSP00000452206.2:p.Asn52His
ENST00000556979.6:c.*826A>C	ENSP00000452378.1:n.*826A>C
ENST00000358664.9:c.373A>C MANE Select	ENSP00000351490.4:p.Asn125His
ENST00000651648.1:c.145-6217A>C	ENSP00000498863.1:n.145-6217A>C
ENST00000284165.10:c.*1217A>C	ENSP00000284165.6:n.*1217A>C
ENST00000341653.6:c.171+17122A>C	ENSP00000342482.2:n.171+17122A>C
ENST00000358402.8:c.346A>C	ENSP00000351175.4:p.Asn116His
ENST00000358664.8:c.373A>C	ENSP00000351490.4:p.Asn125His
ENST00000394606.6:c.*146A>C	ENSP00000378104.2:n.*146A>C
ENST00000553928.5:c.*162A>C	ENSP00000451907.1:n.*162A>C
ENST00000555419.5:c.265A>C	ENSP00000452405.1:p.Asn89His
ENST00000555932.5:c.114A>C	ENSP00000450763.1:p.Pro38=
ENST00000557277.5:c.184A>C	ENSP00000450955.1:p.Asn62His
ENST00000618858.4:c.*162A>C	ENSP00000480127.1:n.*162A>C
NM_001271069.1:c.144+17122A>C	NP_001257998.1:n.144+17122A>C
NM_002382.4:c.373A>C	NP_002373.3:p.Asn125His
NM_145112.2:c.346A>C	NP_660087.1:p.Asn116His
NM_145113.2:c.*162A>C	NP_660088.1:n.*162A>C
NM_197957.3:c.171+17122A>C	NP_932061.1:n.171+17122A>C
NR_073137.1:n.497A>C
XR_429315.2:n.660A>C
XR_943450.1:n.741A>C
XR_943451.1:n.757A>C
XR_943452.1:n.703A>C
NM_001320415.1:c.184A>C	NP_001307344.1:p.Asn62His
XM_017021312.2:c.184A>C	XP_016876801.1:p.Asn62His
XM_017021313.1:c.184A>C	XP_016876802.1:p.Asn62His
XR_001750326.2:n.718A>C
XR_001750327.2:n.637A>C
XR_002957553.1:n.1151A>C
XR_943450.3:n.741A>C
XR_943451.3:n.757A>C
XR_943452.3:n.702A>C
NM_001320415.2:c.184A>C	NP_001307344.1:p.Asn62His
NM_002382.5:c.373A>C MANE Select	NP_002373.3:p.Asn125His
NM_145112.3:c.346A>C	NP_660087.1:p.Asn116His
NM_145113.3:c.*162A>C	NP_660088.1:n.*162A>C
NM_001271069.2:c.144+17122A>C	NP_001257998.1:n.144+17122A>C
NM_197957.4:c.171+17122A>C	NP_932061.1:n.171+17122A>C