Canonical Allele Identifier: CA1144033094
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021589C= , CM000663.2:g.94021589C= GRCh38
NC_000001.10:g.94487145C= , CM000663.1:g.94487145C= GRCh37
NC_000001.9:g.94259733C= NCBI36
NG_009073.1:g.104561G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370225.4:c.4848+51G= MANE Select ENSP00000359245.3:n.4848+51G=
ENST00000370225.3:c.4848+51G= ENSP00000359245.3:n.4848+51G=
ENST00000460514.1:n.342+51G=
ENST00000536513.5:c.1224+51G= ENSP00000439707.2:n.1224+51G=
NM_000350.2:c.4848+51G= NP_000341.2:n.4848+51G=
NM_000350.3:c.4848+51G= MANE Select NP_000341.2:n.4848+51G=