Canonical Allele Identifier: CA1181405772
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.93996110T= , CM000663.2:g.93996110T= GRCh38
NC_000001.10:g.94461666T= , CM000663.1:g.94461666T= GRCh37
NC_000001.9:g.94234254T= NCBI36
NG_009073.1:g.130040A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.6815A= MANE Select ENSP00000359245.3:p.Gln2272=
ENST00000370225.3:c.6815A= ENSP00000359245.3:p.Gln2272=
ENST00000536513.5:c.3191A= ENSP00000439707.2:p.Gln1064=
NM_000350.2:c.6815A= NP_000341.2:p.Gln2272=
NM_000350.3:c.6815A= MANE Select NP_000341.2:p.Gln2272=