Canonical Allele Identifier: CA493168764
Gene: ABCA3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.2376429C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2326428C>T , CM000678.2:g.2326428C>T GRCh38
NC_000016.9:g.2376429C>T , CM000678.1:g.2376429C>T GRCh37
NC_000016.8:g.2316430C>T NCBI36
NG_011790.1:g.19319G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.39G>A MANE Select ENSP00000301732.5:p.Lys13=
ENST00000301732.9:c.39G>A ENSP00000301732.5:p.Lys13=
ENST00000382381.7:c.39G>A ENSP00000371818.3:p.Lys13=
ENST00000563623.5:n.602G>A
ENST00000567910.1:c.39G>A ENSP00000454397.1:p.Lys13=
NM_001089.2:c.39G>A NP_001080.2:p.Lys13=
NM_001089.3:c.39G>A MANE Select NP_001080.2:p.Lys13=