Canonical Allele Identifier: CA1181397633
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94000982C= , CM000663.2:g.94000982C= GRCh38
NC_000001.10:g.94466538C= , CM000663.1:g.94466538C= GRCh37
NC_000001.9:g.94239126C= NCBI36
NG_009073.1:g.125168G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6386+20G= MANE Select ENSP00000359245.3:n.6386+20G=
ENST00000370225.3:c.6386+20G= ENSP00000359245.3:n.6386+20G=
ENST00000536513.5:c.2762+20G= ENSP00000439707.2:n.2762+20G=
NM_000350.2:c.6386+20G= NP_000341.2:n.6386+20G=
NM_000350.3:c.6386+20G= MANE Select NP_000341.2:n.6386+20G=