Canonical Allele Identifier: CA2202176728
Gene: ABCA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2337184G= , CM000678.2:g.2337184G= GRCh38
NC_000016.9:g.2387185G= , CM000678.1:g.2387185G= GRCh37
NC_000016.8:g.2327186G= NCBI36
NG_011790.1:g.8563C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.-539+3389C= MANE Select ENSP00000301732.5:n.-539+3389C=
ENST00000301732.9:c.-539+3389C= ENSP00000301732.5:n.-539+3389C=
ENST00000382381.7:c.-539+3389C= ENSP00000371818.3:n.-539+3389C=
ENST00000563623.5:n.25+3389C=
NM_001089.2:c.-539+3389C= NP_001080.2:n.-539+3389C=
NM_001089.3:c.-539+3389C= MANE Select NP_001080.2:n.-539+3389C=