Canonical Allele Identifier: CA341277822
Gene: ABCA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94056684C>A , CM000663.2:g.94056684C>A GRCh38
NC_000001.10:g.94522240C>A , CM000663.1:g.94522240C>A GRCh37
NC_000001.9:g.94294828C>A NCBI36
NG_009073.1:g.69466G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.2299G>T MANE Select ENSP00000359245.3:p.Val767Phe
ENST00000649773.1:c.2161-1369G>T ENSP00000496882.1:n.2161-1369G>T
ENST00000370225.3:c.2299G>T ENSP00000359245.3:p.Val767Phe
ENST00000536513.5:c.-65+6490G>T ENSP00000439707.2:n.-65+6490G>T
NM_000350.2:c.2299G>T NP_000341.2:p.Val767Phe
NM_000350.3:c.2299G>T MANE Select NP_000341.2:p.Val767Phe