Canonical Allele Identifier: CA2142950849
Gene: MAX HGNC NCBI

Linked Data

dbSNP Id: rs2063021011

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.65074790_65074798del , CM000676.2:g.65074790_65074798del GRCh38
NC_000014.8:g.65541508_65541516del , CM000676.1:g.65541508_65541516del GRCh37
NC_000014.7:g.64611261_64611269del NCBI36
NG_029830.1:g.32715_32723del , LRG_530:g.32715_32723del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651648.1:c.145-4426_145-4418del ENSP00000498863.1:n.145-4426_145-4418del
ENST00000341653.6:c.171+18913_171+18921del ENSP00000342482.2:n.171+18913_171+18921del
NM_001271069.1:c.144+18913_144+18921del NP_001257998.1:n.144+18913_144+18921del
NM_197957.3:c.171+18913_171+18921del NP_932061.1:n.171+18913_171+18921del
NM_001271069.2:c.144+18913_144+18921del NP_001257998.1:n.144+18913_144+18921del
NM_197957.4:c.171+18913_171+18921del NP_932061.1:n.171+18913_171+18921del