Canonical Allele Identifier: CA1181408825
Gene: ABCA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021842A= , CM000663.2:g.94021842A= GRCh38
NC_000001.10:g.94487398A= , CM000663.1:g.94487398A= GRCh37
NC_000001.9:g.94259986A= NCBI36
NG_009073.1:g.104308T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4773+4T= MANE Select ENSP00000359245.3:n.4773+4T=
ENST00000370225.3:c.4773+4T= ENSP00000359245.3:n.4773+4T=
ENST00000460514.1:n.267+4T=
ENST00000536513.5:c.1149+4T= ENSP00000439707.2:n.1149+4T=
NM_000350.2:c.4773+4T= NP_000341.2:n.4773+4T=
NM_000350.3:c.4773+4T= MANE Select NP_000341.2:n.4773+4T=
Search 100 bp 5'
Search 100 bp 3'