Canonical Allele Identifier: CA2202178578
Gene: ABCA3 HGNC NCBI
ABCA17P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340530C= , CM000678.2:g.2340530C= GRCh38
NC_000016.9:g.2390531C= , CM000678.1:g.2390531C= GRCh37
NC_000016.8:g.2330532C= NCBI36
NG_011790.1:g.5217G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.-539+43G= (ABCA3) MANE Select ENSP00000301732.5:n.-539+43G=
ENST00000640929.1:n.42+1199C= (ABCA17P)
ENST00000301732.9:c.-539+43G= (ABCA3) ENSP00000301732.5:n.-539+43G=
ENST00000382381.7:c.-539+43G= (ABCA3) ENSP00000371818.3:n.-539+43G=
ENST00000512848.5:n.182+1199C= (ABCA17P)
ENST00000563623.5:n.25+43G= (ABCA3)
NM_001089.2:c.-539+43G= (ABCA3) NP_001080.2:n.-539+43G=
NM_001089.3:c.-539+43G= (ABCA3) MANE Select NP_001080.2:n.-539+43G=