Canonical Allele Identifier: CA2590066762
Gene: ABCA3 HGNC NCBI
ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2141757098
gnomAD v3: 16-2340514-G-A
gnomAD v4: 16-2340514-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340514G>A , CM000678.2:g.2340514G>A GRCh38
NC_000016.9:g.2390515G>A , CM000678.1:g.2390515G>A GRCh37
NC_000016.8:g.2330516G>A NCBI36
NG_011790.1:g.5233C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301732.10:c.-539+59C>T (ABCA3) MANE Select ENSP00000301732.5:n.-539+59C>T
ENST00000640929.1:n.42+1183G>A (ABCA17P)
ENST00000301732.9:c.-539+59C>T (ABCA3) ENSP00000301732.5:n.-539+59C>T
ENST00000382381.7:c.-539+59C>T (ABCA3) ENSP00000371818.3:n.-539+59C>T
ENST00000512848.5:n.182+1183G>A (ABCA17P)
ENST00000563623.5:n.25+59C>T (ABCA3)
NM_001089.2:c.-539+59C>T (ABCA3) NP_001080.2:n.-539+59C>T
NM_001089.3:c.-539+59C>T (ABCA3) MANE Select NP_001080.2:n.-539+59C>T