Canonical Allele Identifier: CA1181408367
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021464A= , CM000663.2:g.94021464A= GRCh38
NC_000001.10:g.94487020A= , CM000663.1:g.94487020A= GRCh37
NC_000001.9:g.94259608A= NCBI36
NG_009073.1:g.104686T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4849-55T= MANE Select ENSP00000359245.3:n.4849-55T=
ENST00000370225.3:c.4849-55T= ENSP00000359245.3:n.4849-55T=
ENST00000460514.1:n.343-55T=
ENST00000536513.5:c.1225-55T= ENSP00000439707.2:n.1225-55T=
NM_000350.2:c.4849-55T= NP_000341.2:n.4849-55T=
NM_000350.3:c.4849-55T= MANE Select NP_000341.2:n.4849-55T=