Canonical Allele Identifier: CA394304412
Gene: ABCA3 HGNC NCBI

Linked Data

gnomAD v4: 16-2277927-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2277927G>T , CM000678.2:g.2277927G>T GRCh38
NC_000016.9:g.2327928G>T , CM000678.1:g.2327928G>T GRCh37
NC_000016.8:g.2267929G>T NCBI36
NG_011790.1:g.67820C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.4861C>A MANE Select ENSP00000301732.5:p.Gln1621Lys
ENST00000301732.9:c.4861C>A ENSP00000301732.5:p.Gln1621Lys
ENST00000382381.7:c.4687C>A ENSP00000371818.3:p.Gln1563Lys
NM_001089.2:c.4861C>A NP_001080.2:p.Gln1621Lys
NM_001089.3:c.4861C>A MANE Select NP_001080.2:p.Gln1621Lys