Canonical Allele Identifier: CA2575554478

Gene: MAX

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65076538_65076539insC , CM000676.2:g.65076538_65076539insC	GRCh38
NC_000014.8:g.65543256_65543257insC , CM000676.1:g.65543256_65543257insC	GRCh37
NC_000014.7:g.64613009_64613010insC	NCBI36
NG_029830.1:g.30971_30972insG , LRG_530:g.30971_30972insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556892.6:c.201_202insG	ENSP00000452206.2:p.Ser68GlufsTer5
ENST00000556979.6:c.*873_*874insG	ENSP00000452378.1:n.*873_*874insG
ENST00000358664.9:c.420_421insG MANE Select	ENSP00000351490.4:p.Ser141GlufsTer5
ENST00000651648.1:c.145-6170_145-6169insG	ENSP00000498863.1:n.145-6170_145-6169insG
ENST00000284165.10:c.*1264_*1265insG	ENSP00000284165.6:n.*1264_*1265insG
ENST00000341653.6:c.171+17169_171+17170insG	ENSP00000342482.2:n.171+17169_171+17170insG
ENST00000358402.8:c.393_394insG	ENSP00000351175.4:p.Ser132GlufsTer5
ENST00000358664.8:c.420_421insG	ENSP00000351490.4:p.Ser141GlufsTer5
ENST00000394606.6:c.*193_*194insG	ENSP00000378104.2:n.*193_*194insG
ENST00000553928.5:c.*209_*210insG	ENSP00000451907.1:n.*209_*210insG
ENST00000555419.5:c.312_313insG	ENSP00000452405.1:p.Ser105GlufsTer5
ENST00000555932.5:c.161_162insG	ENSP00000450763.1:p.Ala55SerfsTer21
ENST00000557277.5:c.231_232insG	ENSP00000450955.1:p.Ser78GlufsTer5
ENST00000618858.4:c.*209_*210insG	ENSP00000480127.1:n.*209_*210insG
NM_001271069.1:c.144+17169_144+17170insG	NP_001257998.1:n.144+17169_144+17170insG
NM_002382.4:c.420_421insG	NP_002373.3:p.Ser141GlufsTer5
NM_145112.2:c.393_394insG	NP_660087.1:p.Ser132GlufsTer5
NM_145113.2:c.*209_*210insG	NP_660088.1:n.*209_*210insG
NM_197957.3:c.171+17169_171+17170insG	NP_932061.1:n.171+17169_171+17170insG
NR_073137.1:n.544_545insG
XR_429315.2:n.707_708insG
NM_001320415.1:c.231_232insG	NP_001307344.1:p.Ser78GlufsTer5
XM_017021312.2:c.231_232insG	XP_016876801.1:p.Ser78GlufsTer5
XM_017021313.1:c.231_232insG	XP_016876802.1:p.Ser78GlufsTer5
XR_001750326.2:n.765_766insG
XR_001750327.2:n.684_685insG
XR_002957553.1:n.1198_1199insG
XR_943450.3:n.788_789insG
XR_943451.3:n.804_805insG
XR_943452.3:n.749_750insG
NM_001320415.2:c.231_232insG	NP_001307344.1:p.Ser78GlufsTer5
NM_002382.5:c.420_421insG MANE Select	NP_002373.3:p.Ser141GlufsTer5
NM_145112.3:c.393_394insG	NP_660087.1:p.Ser132GlufsTer5
NM_145113.3:c.*209_*210insG	NP_660088.1:n.*209_*210insG
NM_001271069.2:c.144+17169_144+17170insG	NP_001257998.1:n.144+17169_144+17170insG
NM_197957.4:c.171+17169_171+17170insG	NP_932061.1:n.171+17169_171+17170insG