Canonical Allele Identifier: CA2646650029
Gene: ABCA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043491_94043493del , CM000663.2:g.94043491_94043493del GRCh38
NC_000001.10:g.94509047_94509049del , CM000663.1:g.94509047_94509049del GRCh37
NC_000001.9:g.94281635_94281637del NCBI36
NG_009073.1:g.82659_82661del

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3051-16_3051-14del MANE Select ENSP00000359245.3:n.3051-16_3051-14del
ENST00000370225.3:c.3051-16_3051-14del ENSP00000359245.3:n.3051-16_3051-14del
ENST00000536513.5:c.-64-3402_-64-3400del ENSP00000439707.2:n.-64-3402_-64-3400del
NM_000350.2:c.3051-16_3051-14del NP_000341.2:n.3051-16_3051-14del
NM_000350.3:c.3051-16_3051-14del MANE Select NP_000341.2:n.3051-16_3051-14del