Canonical Allele Identifier: CA2202169392
Gene: ABCA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2326369T= , CM000678.2:g.2326369T= GRCh38
NC_000016.9:g.2376370T= , CM000678.1:g.2376370T= GRCh37
NC_000016.8:g.2316371T= NCBI36
NG_011790.1:g.19378A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.54+44A= MANE Select ENSP00000301732.5:n.54+44A=
ENST00000301732.9:c.54+44A= ENSP00000301732.5:n.54+44A=
ENST00000382381.7:c.54+44A= ENSP00000371818.3:n.54+44A=
ENST00000563623.5:n.617+44A=
ENST00000567910.1:c.54+44A= ENSP00000454397.1:n.54+44A=
NM_001089.2:c.54+44A= NP_001080.2:n.54+44A=
NM_001089.3:c.54+44A= MANE Select NP_001080.2:n.54+44A=