Canonical Allele Identifier: CA914057266
Gene: ABCA3 HGNC NCBI
ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs1567360253
gnomAD v2: 16-2390615-T-C
gnomAD v3: 16-2340614-T-C
gnomAD v4: 16-2340614-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340614T>C , CM000678.2:g.2340614T>C GRCh38
NC_000016.9:g.2390615T>C , CM000678.1:g.2390615T>C GRCh37
NC_000016.8:g.2330616T>C NCBI36
NG_011790.1:g.5133A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.-580A>G (ABCA3) MANE Select ENSP00000301732.5:n.-580A>G
ENST00000640929.1:n.42+1283T>C (ABCA17P)
ENST00000301732.9:c.-580A>G (ABCA3) ENSP00000301732.5:n.-580A>G
ENST00000382381.7:c.-580A>G (ABCA3) ENSP00000371818.3:n.-580A>G
ENST00000512848.5:n.182+1283T>C (ABCA17P)
NM_001089.2:c.-580A>G (ABCA3) NP_001080.2:n.-580A>G
NM_001089.3:c.-580A>G (ABCA3) MANE Select NP_001080.2:n.-580A>G