Canonical Allele Identifier: CA2202176741
Gene: ABCA3 HGNC NCBI

Linked Data

dbSNP Id: rs2093753224

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2337209_2337210dup , CM000678.2:g.2337209_2337210dup GRCh38
NC_000016.9:g.2387210_2387211dup , CM000678.1:g.2387210_2387211dup GRCh37
NC_000016.8:g.2327211_2327212dup NCBI36
NG_011790.1:g.8538_8539dup

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.-539+3364_-539+3365dup MANE Select ENSP00000301732.5:n.-539+3364_-539+3365dup
ENST00000301732.9:c.-539+3364_-539+3365dup ENSP00000301732.5:n.-539+3364_-539+3365dup
ENST00000382381.7:c.-539+3364_-539+3365dup ENSP00000371818.3:n.-539+3364_-539+3365dup
ENST00000563623.5:n.25+3364_25+3365dup
NM_001089.2:c.-539+3364_-539+3365dup NP_001080.2:n.-539+3364_-539+3365dup
NM_001089.3:c.-539+3364_-539+3365dup MANE Select NP_001080.2:n.-539+3364_-539+3365dup