Canonical Allele Identifier: CA1181447925
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94111851A= , CM000663.2:g.94111851A= GRCh38
NC_000001.10:g.94577407A= , CM000663.1:g.94577407A= GRCh37
NC_000001.9:g.94349995A= NCBI36
NG_009073.1:g.14299T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.161-272T= MANE Select ENSP00000359245.3:n.161-272T=
ENST00000649773.1:c.161-272T= ENSP00000496882.1:n.161-272T=
ENST00000370225.3:c.161-272T= ENSP00000359245.3:n.161-272T=
NM_000350.2:c.161-272T= NP_000341.2:n.161-272T=
NM_000350.3:c.161-272T= MANE Select NP_000341.2:n.161-272T=