Canonical Allele Identifier: CA2202146052
Gene: ABCA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2277939T= , CM000678.2:g.2277939T= GRCh38
NC_000016.9:g.2327940T= , CM000678.1:g.2327940T= GRCh37
NC_000016.8:g.2267941T= NCBI36
NG_011790.1:g.67808A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301732.10:c.4849A= MANE Select ENSP00000301732.5:p.Ser1617=
ENST00000301732.9:c.4849A= ENSP00000301732.5:p.Ser1617=
ENST00000382381.7:c.4675A= ENSP00000371818.3:p.Ser1559=
NM_001089.2:c.4849A= NP_001080.2:p.Ser1617=
NM_001089.3:c.4849A= MANE Select NP_001080.2:p.Ser1617=