Canonical Allele Identifier: CA1141892569
Gene: ABCA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94111365C= , CM000663.2:g.94111365C= GRCh38
NC_000001.10:g.94576921C= , CM000663.1:g.94576921C= GRCh37
NC_000001.9:g.94349509C= NCBI36
NG_009073.1:g.14785G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.302+73G= MANE Select ENSP00000359245.3:n.302+73G=
ENST00000649773.1:c.302+73G= ENSP00000496882.1:n.302+73G=
ENST00000370225.3:c.302+73G= ENSP00000359245.3:n.302+73G=
NM_000350.2:c.302+73G= NP_000341.2:n.302+73G=
NM_000350.3:c.302+73G= MANE Select NP_000341.2:n.302+73G=
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