Canonical Allele Identifier: CA1181418922
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94062890C= , CM000663.2:g.94062890C= GRCh38
NC_000001.10:g.94528446C= , CM000663.1:g.94528446C= GRCh37
NC_000001.9:g.94301034C= NCBI36
NG_009073.1:g.63260G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1761-137G= MANE Select ENSP00000359245.3:n.1761-137G=
ENST00000649773.1:c.1761-137G= ENSP00000496882.1:n.1761-137G=
ENST00000370225.3:c.1761-137G= ENSP00000359245.3:n.1761-137G=
ENST00000536513.5:c.-65+284G= ENSP00000439707.2:n.-65+284G=
NM_000350.2:c.1761-137G= NP_000341.2:n.1761-137G=
NM_000350.3:c.1761-137G= MANE Select NP_000341.2:n.1761-137G=