Canonical Allele Identifier: CA1181415099
Gene: ABCA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94030884C= , CM000663.2:g.94030884C= GRCh38
NC_000001.10:g.94496440C= , CM000663.1:g.94496440C= GRCh37
NC_000001.9:g.94269028C= NCBI36
NG_009073.1:g.95266G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4253+112G= MANE Select ENSP00000359245.3:n.4253+112G=
ENST00000370225.3:c.4253+112G= ENSP00000359245.3:n.4253+112G=
ENST00000536513.5:c.629+112G= ENSP00000439707.2:n.629+112G=
NM_000350.2:c.4253+112G= NP_000341.2:n.4253+112G=
NM_000350.3:c.4253+112G= MANE Select NP_000341.2:n.4253+112G=
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