Canonical Allele Identifier: CA386614172
Gene: ACADS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.121174912A>C (hg19) chr12:g.120737109A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120737109A>C , CM000674.2:g.120737109A>C GRCh38
NC_000012.11:g.121174912A>C , CM000674.1:g.121174912A>C GRCh37
NC_000012.10:g.119659295A>C NCBI36
NG_007991.1:g.16342A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.334A>C MANE Select ENSP00000242592.4:p.Thr112Pro
ENST00000242592.8:c.334A>C ENSP00000242592.4:p.Thr112Pro
ENST00000411593.2:c.334A>C ENSP00000401045.2:p.Thr112Pro
ENST00000539690.1:n.446A>C
NM_000017.3:c.334A>C NP_000008.1:p.Thr112Pro
NM_001302554.1:c.334A>C NP_001289483.1:p.Thr112Pro
NM_000017.4:c.334A>C MANE Select NP_000008.1:p.Thr112Pro
NM_001302554.2:c.334A>C NP_001289483.1:p.Thr112Pro
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