Canonical Allele Identifier: CA1181406362
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93997787A= , CM000663.2:g.93997787A= GRCh38
NC_000001.10:g.94463343A= , CM000663.1:g.94463343A= GRCh37
NC_000001.9:g.94235931A= NCBI36
NG_009073.1:g.128363T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6729+74T= MANE Select ENSP00000359245.3:n.6729+74T=
ENST00000370225.3:c.6729+74T= ENSP00000359245.3:n.6729+74T=
ENST00000536513.5:c.3105+74T= ENSP00000439707.2:n.3105+74T=
NM_000350.2:c.6729+74T= NP_000341.2:n.6729+74T=
NM_000350.3:c.6729+74T= MANE Select NP_000341.2:n.6729+74T=