Canonical Allele Identifier: CA2631192682
Gene: ABCA3 HGNC NCBI
ABCA17P HGNC NCBI

Linked Data

gnomAD v4: 16-2340522-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340522C>T , CM000678.2:g.2340522C>T GRCh38
NC_000016.9:g.2390523C>T , CM000678.1:g.2390523C>T GRCh37
NC_000016.8:g.2330524C>T NCBI36
NG_011790.1:g.5225G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.-539+51G>A (ABCA3) MANE Select ENSP00000301732.5:n.-539+51G>A
ENST00000640929.1:n.42+1191C>T (ABCA17P)
ENST00000301732.9:c.-539+51G>A (ABCA3) ENSP00000301732.5:n.-539+51G>A
ENST00000382381.7:c.-539+51G>A (ABCA3) ENSP00000371818.3:n.-539+51G>A
ENST00000512848.5:n.182+1191C>T (ABCA17P)
ENST00000563623.5:n.25+51G>A (ABCA3)
NM_001089.2:c.-539+51G>A (ABCA3) NP_001080.2:n.-539+51G>A
NM_001089.3:c.-539+51G>A (ABCA3) MANE Select NP_001080.2:n.-539+51G>A