Canonical Allele Identifier: CA2202178398
Gene: ABCA3 HGNC NCBI
ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2093758743

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340321A>C , CM000678.2:g.2340321A>C GRCh38
NC_000016.9:g.2390322A>C , CM000678.1:g.2390322A>C GRCh37
NC_000016.8:g.2330323A>C NCBI36
NG_011790.1:g.5426T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.-539+252T>G (ABCA3) MANE Select ENSP00000301732.5:n.-539+252T>G
ENST00000640929.1:n.42+990A>C (ABCA17P)
ENST00000301732.9:c.-539+252T>G (ABCA3) ENSP00000301732.5:n.-539+252T>G
ENST00000382381.7:c.-539+252T>G (ABCA3) ENSP00000371818.3:n.-539+252T>G
ENST00000512848.5:n.182+990A>C (ABCA17P)
ENST00000563623.5:n.25+252T>G (ABCA3)
NM_001089.2:c.-539+252T>G (ABCA3) NP_001080.2:n.-539+252T>G
NM_001089.3:c.-539+252T>G (ABCA3) MANE Select NP_001080.2:n.-539+252T>G