Canonical Allele Identifier: CA2202146169
Gene: ABCA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2278200C= , CM000678.2:g.2278200C= GRCh38
NC_000016.9:g.2328201C= , CM000678.1:g.2328201C= GRCh37
NC_000016.8:g.2268202C= NCBI36
NG_011790.1:g.67547G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4718+88G= MANE Select ENSP00000301732.5:n.4718+88G=
ENST00000301732.9:c.4718+88G= ENSP00000301732.5:n.4718+88G=
ENST00000382381.7:c.4544+88G= ENSP00000371818.3:n.4544+88G=
NM_001089.2:c.4718+88G= NP_001080.2:n.4718+88G=
NM_001089.3:c.4718+88G= MANE Select NP_001080.2:n.4718+88G=