Canonical Allele Identifier: CA394316631
Gene: ABCA3 HGNC NCBI

Linked Data

gnomAD v4: 16-2285504-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2285504A>T , CM000678.2:g.2285504A>T GRCh38
NC_000016.9:g.2335505A>T , CM000678.1:g.2335505A>T GRCh37
NC_000016.8:g.2275506A>T NCBI36
NG_011790.1:g.60243T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.3421T>A MANE Select ENSP00000301732.5:p.Phe1141Ile
ENST00000301732.9:c.3421T>A ENSP00000301732.5:p.Phe1141Ile
ENST00000382381.7:c.3247T>A ENSP00000371818.3:p.Phe1083Ile
NM_001089.2:c.3421T>A NP_001080.2:p.Phe1141Ile
NM_001089.3:c.3421T>A MANE Select NP_001080.2:p.Phe1141Ile