Canonical Allele Identifier: CA341286488

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94496667G>T (hg19) ; chr1:g.94031111G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94031111G>T , CM000663.2:g.94031111G>T	GRCh38
NC_000001.10:g.94496667G>T , CM000663.1:g.94496667G>T	GRCh37
NC_000001.9:g.94269255G>T	NCBI36
NG_009073.1:g.95039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.4138C>A MANE Select	ENSP00000359245.3:p.Pro1380Thr
ENST00000370225.3:c.4138C>A	ENSP00000359245.3:p.Pro1380Thr
ENST00000536513.5:c.514C>A	ENSP00000439707.2:p.Pro172Thr
NM_000350.2:c.4138C>A	NP_000341.2:p.Pro1380Thr
NM_000350.3:c.4138C>A MANE Select	NP_000341.2:p.Pro1380Thr