Canonical Allele Identifier: CA1181428067
Gene: ABCA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060692T= , CM000663.2:g.94060692T= GRCh38
NC_000001.10:g.94526248T= , CM000663.1:g.94526248T= GRCh37
NC_000001.9:g.94298836T= NCBI36
NG_009073.1:g.65458A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2005A= MANE Select ENSP00000359245.3:p.Met669=
ENST00000649773.1:c.2005A= ENSP00000496882.1:p.Met669=
ENST00000370225.3:c.2005A= ENSP00000359245.3:p.Met669=
ENST00000472033.1:n.125A=
ENST00000536513.5:c.-65+2482A= ENSP00000439707.2:n.-65+2482A=
NM_000350.2:c.2005A= NP_000341.2:p.Met669=
NM_000350.3:c.2005A= MANE Select NP_000341.2:p.Met669=
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