Canonical Allele Identifier: CA197917

Gene: MAX

Linked Data

• ClinVar Variation Id: 187544
• ClinVar RCV Id: RCV000167282
• dbSNP Id: rs786203812
• MyVariant Identifiers: chr14:g.65543338G>T (hg19) ; chr14:g.65076620G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076620G>T , CM000676.2:g.65076620G>T	GRCh38
NC_000014.8:g.65543338G>T , CM000676.1:g.65543338G>T	GRCh37
NC_000014.7:g.64613091G>T	NCBI36
NG_029830.1:g.30890C>A , LRG_530:g.30890C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.120C>A	ENSP00000452206.2:p.Thr40=
ENST00000556979.6:c.*792C>A	ENSP00000452378.1:n.*792C>A
ENST00000358664.9:c.339C>A MANE Select	ENSP00000351490.4:p.Thr113=
ENST00000651648.1:c.145-6251C>A	ENSP00000498863.1:n.145-6251C>A
ENST00000284165.10:c.*1183C>A	ENSP00000284165.6:n.*1183C>A
ENST00000341653.6:c.171+17088C>A	ENSP00000342482.2:n.171+17088C>A
ENST00000358402.8:c.312C>A	ENSP00000351175.4:p.Thr104=
ENST00000358664.8:c.339C>A	ENSP00000351490.4:p.Thr113=
ENST00000394606.6:c.*112C>A	ENSP00000378104.2:n.*112C>A
ENST00000553928.5:c.*128C>A	ENSP00000451907.1:n.*128C>A
ENST00000555419.5:c.231C>A	ENSP00000452405.1:p.Thr77=
ENST00000555932.5:c.80C>A	ENSP00000450763.1:p.Pro27Gln
ENST00000556892.5:c.120C>A	ENSP00000452206.1:p.Thr40=
ENST00000557277.5:c.150C>A	ENSP00000450955.1:p.Thr50=
ENST00000618858.4:c.*128C>A	ENSP00000480127.1:n.*128C>A
NM_001271069.1:c.144+17088C>A	NP_001257998.1:n.144+17088C>A
NM_002382.4:c.339C>A	NP_002373.3:p.Thr113=
NM_145112.2:c.312C>A	NP_660087.1:p.Thr104=
NM_145113.2:c.*128C>A	NP_660088.1:n.*128C>A
NM_197957.3:c.171+17088C>A	NP_932061.1:n.171+17088C>A
NR_073137.1:n.463C>A
XR_429315.2:n.626C>A
XR_943450.1:n.707C>A
XR_943451.1:n.723C>A
XR_943452.1:n.669C>A
NM_001320415.1:c.150C>A	NP_001307344.1:p.Thr50=
XM_017021312.2:c.150C>A	XP_016876801.1:p.Thr50=
XM_017021313.1:c.150C>A	XP_016876802.1:p.Thr50=
XR_001750326.2:n.684C>A
XR_001750327.2:n.603C>A
XR_002957553.1:n.1117C>A
XR_943450.3:n.707C>A
XR_943451.3:n.723C>A
XR_943452.3:n.668C>A
NM_001320415.2:c.150C>A	NP_001307344.1:p.Thr50=
NM_002382.5:c.339C>A MANE Select	NP_002373.3:p.Thr113=
NM_145112.3:c.312C>A	NP_660087.1:p.Thr104=
NM_145113.3:c.*128C>A	NP_660088.1:n.*128C>A
NM_001271069.2:c.144+17088C>A	NP_001257998.1:n.144+17088C>A
NM_197957.4:c.171+17088C>A	NP_932061.1:n.171+17088C>A