Canonical Allele Identifier: CA973791770
Gene: ABCA3 HGNC NCBI
ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2093759349
gnomAD v3: 16-2340536-A-C
gnomAD v4: 16-2340536-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340536A>C , CM000678.2:g.2340536A>C GRCh38
NC_000016.9:g.2390537A>C , CM000678.1:g.2390537A>C GRCh37
NC_000016.8:g.2330538A>C NCBI36
NG_011790.1:g.5211T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.-539+37T>G (ABCA3) MANE Select ENSP00000301732.5:n.-539+37T>G
ENST00000640929.1:n.42+1205A>C (ABCA17P)
ENST00000301732.9:c.-539+37T>G (ABCA3) ENSP00000301732.5:n.-539+37T>G
ENST00000382381.7:c.-539+37T>G (ABCA3) ENSP00000371818.3:n.-539+37T>G
ENST00000512848.5:n.182+1205A>C (ABCA17P)
ENST00000563623.5:n.25+37T>G (ABCA3)
NM_001089.2:c.-539+37T>G (ABCA3) NP_001080.2:n.-539+37T>G
NM_001089.3:c.-539+37T>G (ABCA3) MANE Select NP_001080.2:n.-539+37T>G