Canonical Allele Identifier: CA2202166762
Gene: ABCA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2317589C= , CM000678.2:g.2317589C= GRCh38
NC_000016.9:g.2367590C= , CM000678.1:g.2367590C= GRCh37
NC_000016.8:g.2307591C= NCBI36
NG_011790.1:g.28158G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.990+59G= MANE Select ENSP00000301732.5:n.990+59G=
ENST00000301732.9:c.990+59G= ENSP00000301732.5:n.990+59G=
ENST00000382381.7:c.990+59G= ENSP00000371818.3:n.990+59G=
ENST00000563623.5:n.1553+59G=
NM_001089.2:c.990+59G= NP_001080.2:n.990+59G=
NM_001089.3:c.990+59G= MANE Select NP_001080.2:n.990+59G=