Canonical Allele Identifier: CA2142950963
Gene: MAX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65075102_65075103delinsAG , CM000676.2:g.65075102_65075103delinsAG GRCh38
NC_000014.8:g.65541820_65541821delinsAG , CM000676.1:g.65541820_65541821delinsAG GRCh37
NC_000014.7:g.64611573_64611574delinsAG NCBI36
NG_029830.1:g.32407_32408delinsCT , LRG_530:g.32407_32408delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4734_145-4733delinsCT ENSP00000498863.1:n.145-4734_145-4733delinsCT
ENST00000341653.6:c.171+18605_171+18606delinsCT ENSP00000342482.2:n.171+18605_171+18606delinsCT
NM_001271069.1:c.144+18605_144+18606delinsCT NP_001257998.1:n.144+18605_144+18606delinsCT
NM_197957.3:c.171+18605_171+18606delinsCT NP_932061.1:n.171+18605_171+18606delinsCT
NM_001271069.2:c.144+18605_144+18606delinsCT NP_001257998.1:n.144+18605_144+18606delinsCT
NM_197957.4:c.171+18605_171+18606delinsCT NP_932061.1:n.171+18605_171+18606delinsCT