Canonical Allele Identifier: CA2142950977
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075123_65075126delinsCAAG , CM000676.2:g.65075123_65075126delinsCAAG GRCh38
NC_000014.8:g.65541841_65541844delinsCAAG , CM000676.1:g.65541841_65541844delinsCAAG GRCh37
NC_000014.7:g.64611594_64611597delinsCAAG NCBI36
NG_029830.1:g.32384_32387delinsCTTG , LRG_530:g.32384_32387delinsCTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4757_145-4754delinsCTTG ENSP00000498863.1:n.145-4757_145-4754delinsCTTG
ENST00000341653.6:c.171+18582_171+18585delinsCTTG ENSP00000342482.2:n.171+18582_171+18585delinsCTTG
NM_001271069.1:c.144+18582_144+18585delinsCTTG NP_001257998.1:n.144+18582_144+18585delinsCTTG
NM_197957.3:c.171+18582_171+18585delinsCTTG NP_932061.1:n.171+18582_171+18585delinsCTTG
NM_001271069.2:c.144+18582_144+18585delinsCTTG NP_001257998.1:n.144+18582_144+18585delinsCTTG
NM_197957.4:c.171+18582_171+18585delinsCTTG NP_932061.1:n.171+18582_171+18585delinsCTTG