Canonical Allele Identifier: CA386614192
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1267605129

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120737119T>C , CM000674.2:g.120737119T>C GRCh38
NC_000012.11:g.121174922T>C , CM000674.1:g.121174922T>C GRCh37
NC_000012.10:g.119659305T>C NCBI36
NG_007991.1:g.16352T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.344T>C MANE Select ENSP00000242592.4:p.Ile115Thr
ENST00000242592.8:c.344T>C ENSP00000242592.4:p.Ile115Thr
ENST00000411593.2:c.344T>C ENSP00000401045.2:p.Ile115Thr
ENST00000539690.1:n.456T>C
NM_000017.3:c.344T>C NP_000008.1:p.Ile115Thr
NM_001302554.1:c.344T>C NP_001289483.1:p.Ile115Thr
NM_000017.4:c.344T>C MANE Select NP_000008.1:p.Ile115Thr
NM_001302554.2:c.344T>C NP_001289483.1:p.Ile115Thr