Canonical Allele Identifier: CA2744619182
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060886_94060887insAGT , CM000663.2:g.94060886_94060887insAGT GRCh38
NC_000001.10:g.94526442_94526443insAGT , CM000663.1:g.94526442_94526443insAGT GRCh37
NC_000001.9:g.94299030_94299031insAGT NCBI36
NG_009073.1:g.65263_65264insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1938-128_1938-127insACT MANE Select ENSP00000359245.3:n.1938-128_1938-127insACT
ENST00000649773.1:c.1938-128_1938-127insACT ENSP00000496882.1:n.1938-128_1938-127insACT
ENST00000370225.3:c.1938-128_1938-127insACT ENSP00000359245.3:n.1938-128_1938-127insACT
ENST00000472033.1:n.58-128_58-127insACT
ENST00000536513.5:c.-65+2287_-65+2288insACT ENSP00000439707.2:n.-65+2287_-65+2288insACT
NM_000350.2:c.1938-128_1938-127insACT NP_000341.2:n.1938-128_1938-127insACT
NM_000350.3:c.1938-128_1938-127insACT MANE Select NP_000341.2:n.1938-128_1938-127insACT