Canonical Allele Identifier: CA2744619280
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062814_94062815insAGA , CM000663.2:g.94062814_94062815insAGA GRCh38
NC_000001.10:g.94528370_94528371insAGA , CM000663.1:g.94528370_94528371insAGA GRCh37
NC_000001.9:g.94300958_94300959insAGA NCBI36
NG_009073.1:g.63335_63336insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1761-62_1761-61insTCT MANE Select ENSP00000359245.3:n.1761-62_1761-61insTCT
ENST00000649773.1:c.1761-62_1761-61insTCT ENSP00000496882.1:n.1761-62_1761-61insTCT
ENST00000370225.3:c.1761-62_1761-61insTCT ENSP00000359245.3:n.1761-62_1761-61insTCT
ENST00000536513.5:c.-65+359_-65+360insTCT ENSP00000439707.2:n.-65+359_-65+360insTCT
NM_000350.2:c.1761-62_1761-61insTCT NP_000341.2:n.1761-62_1761-61insTCT
NM_000350.3:c.1761-62_1761-61insTCT MANE Select NP_000341.2:n.1761-62_1761-61insTCT