Canonical Allele Identifier: CA1143533238
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94111371T= , CM000663.2:g.94111371T= GRCh38
NC_000001.10:g.94576927T= , CM000663.1:g.94576927T= GRCh37
NC_000001.9:g.94349515T= NCBI36
NG_009073.1:g.14779A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.302+67A= MANE Select ENSP00000359245.3:n.302+67A=
ENST00000649773.1:c.302+67A= ENSP00000496882.1:n.302+67A=
ENST00000370225.3:c.302+67A= ENSP00000359245.3:n.302+67A=
NM_000350.2:c.302+67A= NP_000341.2:n.302+67A=
NM_000350.3:c.302+67A= MANE Select NP_000341.2:n.302+67A=