Canonical Allele Identifier: CA1181395408
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93998126A= , CM000663.2:g.93998126A= GRCh38
NC_000001.10:g.94463682A= , CM000663.1:g.94463682A= GRCh37
NC_000001.9:g.94236270A= NCBI36
NG_009073.1:g.128024T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.6480-16T= MANE Select ENSP00000359245.3:n.6480-16T=
ENST00000370225.3:c.6480-16T= ENSP00000359245.3:n.6480-16T=
ENST00000536513.5:c.2856-16T= ENSP00000439707.2:n.2856-16T=
NM_000350.2:c.6480-16T= NP_000341.2:n.6480-16T=
NM_000350.3:c.6480-16T= MANE Select NP_000341.2:n.6480-16T=