Canonical Allele Identifier: CA2142950851
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs2063021133

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65074799_65074806del , CM000676.2:g.65074799_65074806del GRCh38
NC_000014.8:g.65541517_65541524del , CM000676.1:g.65541517_65541524del GRCh37
NC_000014.7:g.64611270_64611277del NCBI36
NG_029830.1:g.32705_32712del , LRG_530:g.32705_32712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4436_145-4429del ENSP00000498863.1:n.145-4436_145-4429del
ENST00000341653.6:c.171+18903_171+18910del ENSP00000342482.2:n.171+18903_171+18910del
NM_001271069.1:c.144+18903_144+18910del NP_001257998.1:n.144+18903_144+18910del
NM_197957.3:c.171+18903_171+18910del NP_932061.1:n.171+18903_171+18910del
NM_001271069.2:c.144+18903_144+18910del NP_001257998.1:n.144+18903_144+18910del
NM_197957.4:c.171+18903_171+18910del NP_932061.1:n.171+18903_171+18910del