Canonical Allele Identifier: CA341284064
Gene: ABCA4 HGNC NCBI

Linked Data

COSMIC: COSM40999
MyVariant Identifiers: chr1:g.94487500C>A (hg19) chr1:g.94021944C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94021944C>A , CM000663.2:g.94021944C>A GRCh38
NC_000001.10:g.94487500C>A , CM000663.1:g.94487500C>A GRCh37
NC_000001.9:g.94260088C>A NCBI36
NG_009073.1:g.104206G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370225.4:c.4675G>T MANE Select ENSP00000359245.3:p.Gly1559Ter
ENST00000370225.3:c.4675G>T ENSP00000359245.3:p.Gly1559Ter
ENST00000460514.1:n.169G>T
ENST00000536513.5:c.1051G>T ENSP00000439707.2:p.Gly351Ter
NM_000350.2:c.4675G>T NP_000341.2:p.Gly1559Ter
NM_000350.3:c.4675G>T MANE Select NP_000341.2:p.Gly1559Ter
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