Canonical Allele Identifier: CA341278628
Gene: ABCA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060636T>G , CM000663.2:g.94060636T>G GRCh38
NC_000001.10:g.94526192T>G , CM000663.1:g.94526192T>G GRCh37
NC_000001.9:g.94298780T>G NCBI36
NG_009073.1:g.65514A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2061A>C MANE Select ENSP00000359245.3:p.Lys687Asn
ENST00000649773.1:c.2061A>C ENSP00000496882.1:p.Lys687Asn
ENST00000370225.3:c.2061A>C ENSP00000359245.3:p.Lys687Asn
ENST00000472033.1:n.181A>C
ENST00000536513.5:c.-65+2538A>C ENSP00000439707.2:n.-65+2538A>C
NM_000350.2:c.2061A>C NP_000341.2:p.Lys687Asn
NM_000350.3:c.2061A>C MANE Select NP_000341.2:p.Lys687Asn