Canonical Allele Identifier: CA1181422506
Gene: ABCA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94046700C= , CM000663.2:g.94046700C= GRCh38
NC_000001.10:g.94512256C= , CM000663.1:g.94512256C= GRCh37
NC_000001.9:g.94284844C= NCBI36
NG_009073.1:g.79450G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.2918+219G= MANE Select ENSP00000359245.3:n.2918+219G=
ENST00000649773.1:c.2696+219G= ENSP00000496882.1:n.2696+219G=
ENST00000370225.3:c.2918+219G= ENSP00000359245.3:n.2918+219G=
ENST00000536513.5:c.-64-6611G= ENSP00000439707.2:n.-64-6611G=
NM_000350.2:c.2918+219G= NP_000341.2:n.2918+219G=
NM_000350.3:c.2918+219G= MANE Select NP_000341.2:n.2918+219G=
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