Canonical Allele Identifier: CA1181398763
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94002051C= , CM000663.2:g.94002051C= GRCh38
NC_000001.10:g.94467607C= , CM000663.1:g.94467607C= GRCh37
NC_000001.9:g.94240195C= NCBI36
NG_009073.1:g.124099G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6148-59G= MANE Select ENSP00000359245.3:n.6148-59G=
ENST00000370225.3:c.6148-59G= ENSP00000359245.3:n.6148-59G=
ENST00000465352.1:n.564-59G=
ENST00000536513.5:c.2524-59G= ENSP00000439707.2:n.2524-59G=
NM_000350.2:c.6148-59G= NP_000341.2:n.6148-59G=
NM_000350.3:c.6148-59G= MANE Select NP_000341.2:n.6148-59G=