Canonical Allele Identifier: CA2744619120
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060827_94060828insAGA , CM000663.2:g.94060827_94060828insAGA GRCh38
NC_000001.10:g.94526383_94526384insAGA , CM000663.1:g.94526383_94526384insAGA GRCh37
NC_000001.9:g.94298971_94298972insAGA NCBI36
NG_009073.1:g.65322_65323insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1938-69_1938-68insTCT MANE Select ENSP00000359245.3:n.1938-69_1938-68insTCT
ENST00000649773.1:c.1938-69_1938-68insTCT ENSP00000496882.1:n.1938-69_1938-68insTCT
ENST00000370225.3:c.1938-69_1938-68insTCT ENSP00000359245.3:n.1938-69_1938-68insTCT
ENST00000472033.1:n.58-69_58-68insTCT
ENST00000536513.5:c.-65+2346_-65+2347insTCT ENSP00000439707.2:n.-65+2346_-65+2347insTCT
NM_000350.2:c.1938-69_1938-68insTCT NP_000341.2:n.1938-69_1938-68insTCT
NM_000350.3:c.1938-69_1938-68insTCT MANE Select NP_000341.2:n.1938-69_1938-68insTCT