Canonical Allele Identifier: CA1181395031
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997865T= , CM000663.2:g.93997865T= GRCh38
NC_000001.10:g.94463421T= , CM000663.1:g.94463421T= GRCh37
NC_000001.9:g.94236009T= NCBI36
NG_009073.1:g.128285A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6725A= MANE Select ENSP00000359245.3:p.Asp2242=
ENST00000370225.3:c.6725A= ENSP00000359245.3:p.Asp2242=
ENST00000536513.5:c.3101A= ENSP00000439707.2:p.Asp1034=
NM_000350.2:c.6725A= NP_000341.2:p.Asp2242=
NM_000350.3:c.6725A= MANE Select NP_000341.2:p.Asp2242=