Canonical Allele Identifier: CA418825160

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94496665C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94031109C>G , CM000663.2:g.94031109C>G	GRCh38
NC_000001.10:g.94496665C>G , CM000663.1:g.94496665C>G	GRCh37
NC_000001.9:g.94269253C>G	NCBI36
NG_009073.1:g.95041G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.4140G>C MANE Select	ENSP00000359245.3:p.Pro1380=
ENST00000370225.3:c.4140G>C	ENSP00000359245.3:p.Pro1380=
ENST00000536513.5:c.516G>C	ENSP00000439707.2:p.Pro172=
NM_000350.2:c.4140G>C	NP_000341.2:p.Pro1380=
NM_000350.3:c.4140G>C MANE Select	NP_000341.2:p.Pro1380=