Canonical Allele Identifier: CA1181418907
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062846A= , CM000663.2:g.94062846A= GRCh38
NC_000001.10:g.94528402A= , CM000663.1:g.94528402A= GRCh37
NC_000001.9:g.94300990A= NCBI36
NG_009073.1:g.63304T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1761-93T= MANE Select ENSP00000359245.3:n.1761-93T=
ENST00000649773.1:c.1761-93T= ENSP00000496882.1:n.1761-93T=
ENST00000370225.3:c.1761-93T= ENSP00000359245.3:n.1761-93T=
ENST00000536513.5:c.-65+328T= ENSP00000439707.2:n.-65+328T=
NM_000350.2:c.1761-93T= NP_000341.2:n.1761-93T=
NM_000350.3:c.1761-93T= MANE Select NP_000341.2:n.1761-93T=