Canonical Allele Identifier: CA1141765547
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94046724C= , CM000663.2:g.94046724C= GRCh38
NC_000001.10:g.94512280C= , CM000663.1:g.94512280C= GRCh37
NC_000001.9:g.94284868C= NCBI36
NG_009073.1:g.79426G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2918+195G= MANE Select ENSP00000359245.3:n.2918+195G=
ENST00000649773.1:c.2696+195G= ENSP00000496882.1:n.2696+195G=
ENST00000370225.3:c.2918+195G= ENSP00000359245.3:n.2918+195G=
ENST00000536513.5:c.-64-6635G= ENSP00000439707.2:n.-64-6635G=
NM_000350.2:c.2918+195G= NP_000341.2:n.2918+195G=
NM_000350.3:c.2918+195G= MANE Select NP_000341.2:n.2918+195G=