Canonical Allele Identifier: CA2202169449
Gene: ABCA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2326422G= , CM000678.2:g.2326422G= GRCh38
NC_000016.9:g.2376423G= , CM000678.1:g.2376423G= GRCh37
NC_000016.8:g.2316424G= NCBI36
NG_011790.1:g.19325C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.45C= MANE Select ENSP00000301732.5:p.Tyr15=
ENST00000301732.9:c.45C= ENSP00000301732.5:p.Tyr15=
ENST00000382381.7:c.45C= ENSP00000371818.3:p.Tyr15=
ENST00000563623.5:n.608C=
ENST00000567910.1:c.45C= ENSP00000454397.1:p.Tyr15=
NM_001089.2:c.45C= NP_001080.2:p.Tyr15=
NM_001089.3:c.45C= MANE Select NP_001080.2:p.Tyr15=