Canonical Allele Identifier: CA2202169150
Gene: ABCA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2326176C= , CM000678.2:g.2326176C= GRCh38
NC_000016.9:g.2376177C= , CM000678.1:g.2376177C= GRCh37
NC_000016.8:g.2316178C= NCBI36
NG_011790.1:g.19571G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.153G= MANE Select ENSP00000301732.5:p.Val51=
ENST00000301732.9:c.153G= ENSP00000301732.5:p.Val51=
ENST00000382381.7:c.153G= ENSP00000371818.3:p.Val51=
ENST00000563623.5:n.716G=
ENST00000567910.1:c.153G= ENSP00000454397.1:p.Val51=
NM_001089.2:c.153G= NP_001080.2:p.Val51=
NM_001089.3:c.153G= MANE Select NP_001080.2:p.Val51=