Canonical Allele Identifier: CA1181415009
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030691A= , CM000663.2:g.94030691A= GRCh38
NC_000001.10:g.94496247A= , CM000663.1:g.94496247A= GRCh37
NC_000001.9:g.94268835A= NCBI36
NG_009073.1:g.95459T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4254-165T= MANE Select ENSP00000359245.3:n.4254-165T=
ENST00000370225.3:c.4254-165T= ENSP00000359245.3:n.4254-165T=
ENST00000536513.5:c.630-165T= ENSP00000439707.2:n.630-165T=
NM_000350.2:c.4254-165T= NP_000341.2:n.4254-165T=
NM_000350.3:c.4254-165T= MANE Select NP_000341.2:n.4254-165T=