Canonical Allele Identifier: CA341278755
Gene: ABCA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94060695A>T , CM000663.2:g.94060695A>T GRCh38
NC_000001.10:g.94526251A>T , CM000663.1:g.94526251A>T GRCh37
NC_000001.9:g.94298839A>T NCBI36
NG_009073.1:g.65455T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2002T>A MANE Select ENSP00000359245.3:p.Ser668Thr
ENST00000649773.1:c.2002T>A ENSP00000496882.1:p.Ser668Thr
ENST00000370225.3:c.2002T>A ENSP00000359245.3:p.Ser668Thr
ENST00000472033.1:n.122T>A
ENST00000536513.5:c.-65+2479T>A ENSP00000439707.2:n.-65+2479T>A
NM_000350.2:c.2002T>A NP_000341.2:p.Ser668Thr
NM_000350.3:c.2002T>A MANE Select NP_000341.2:p.Ser668Thr