Canonical Allele Identifier: CA1181420889
Gene: ABCA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94043392A= , CM000663.2:g.94043392A= GRCh38
NC_000001.10:g.94508948A= , CM000663.1:g.94508948A= GRCh37
NC_000001.9:g.94281536A= NCBI36
NG_009073.1:g.82758T=

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.3134T= MANE Select ENSP00000359245.3:p.Met1045=
ENST00000370225.3:c.3134T= ENSP00000359245.3:p.Met1045=
ENST00000536513.5:c.-64-3303T= ENSP00000439707.2:n.-64-3303T=
NM_000350.2:c.3134T= NP_000341.2:p.Met1045=
NM_000350.3:c.3134T= MANE Select NP_000341.2:p.Met1045=