Canonical Allele Identifier: CA341278916
Gene: ABCA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.94526297G>T (hg19) chr1:g.94060741G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060741G>T , CM000663.2:g.94060741G>T GRCh38
NC_000001.10:g.94526297G>T , CM000663.1:g.94526297G>T GRCh37
NC_000001.9:g.94298885G>T NCBI36
NG_009073.1:g.65409C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.1956C>A MANE Select ENSP00000359245.3:p.Asn652Lys
ENST00000649773.1:c.1956C>A ENSP00000496882.1:p.Asn652Lys
ENST00000370225.3:c.1956C>A ENSP00000359245.3:p.Asn652Lys
ENST00000472033.1:n.76C>A
ENST00000536513.5:c.-65+2433C>A ENSP00000439707.2:n.-65+2433C>A
NM_000350.2:c.1956C>A NP_000341.2:p.Asn652Lys
NM_000350.3:c.1956C>A MANE Select NP_000341.2:p.Asn652Lys
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