Canonical Allele Identifier: CA2744619285
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062817_94062818insA , CM000663.2:g.94062817_94062818insA GRCh38
NC_000001.10:g.94528373_94528374insA , CM000663.1:g.94528373_94528374insA GRCh37
NC_000001.9:g.94300961_94300962insA NCBI36
NG_009073.1:g.63332_63333insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1761-65_1761-64insT MANE Select ENSP00000359245.3:n.1761-65_1761-64insT
ENST00000649773.1:c.1761-65_1761-64insT ENSP00000496882.1:n.1761-65_1761-64insT
ENST00000370225.3:c.1761-65_1761-64insT ENSP00000359245.3:n.1761-65_1761-64insT
ENST00000536513.5:c.-65+356_-65+357insT ENSP00000439707.2:n.-65+356_-65+357insT
NM_000350.2:c.1761-65_1761-64insT NP_000341.2:n.1761-65_1761-64insT
NM_000350.3:c.1761-65_1761-64insT MANE Select NP_000341.2:n.1761-65_1761-64insT