Canonical Allele Identifier: CA341292483

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94508936G>A (hg19) ; chr1:g.94043380G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94043380G>A , CM000663.2:g.94043380G>A	GRCh38
NC_000001.10:g.94508936G>A , CM000663.1:g.94508936G>A	GRCh37
NC_000001.9:g.94281524G>A	NCBI36
NG_009073.1:g.82770C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.3146C>T MANE Select	ENSP00000359245.3:p.Thr1049Ile
ENST00000370225.3:c.3146C>T	ENSP00000359245.3:p.Thr1049Ile
ENST00000536513.5:c.-64-3291C>T	ENSP00000439707.2:n.-64-3291C>T
NM_000350.2:c.3146C>T	NP_000341.2:p.Thr1049Ile
NM_000350.3:c.3146C>T MANE Select	NP_000341.2:p.Thr1049Ile