Canonical Allele Identifier: CA386613923
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1341210459

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120736986G>A , CM000674.2:g.120736986G>A GRCh38
NC_000012.11:g.121174789G>A , CM000674.1:g.121174789G>A GRCh37
NC_000012.10:g.119659172G>A NCBI36
NG_007991.1:g.16219G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.211G>A MANE Select ENSP00000242592.4:p.Val71Met
ENST00000242592.8:c.211G>A ENSP00000242592.4:p.Val71Met
ENST00000411593.2:c.211G>A ENSP00000401045.2:p.Val71Met
ENST00000539690.1:n.323G>A
NM_000017.3:c.211G>A NP_000008.1:p.Val71Met
NM_001302554.1:c.211G>A NP_001289483.1:p.Val71Met
NM_000017.4:c.211G>A MANE Select NP_000008.1:p.Val71Met
NM_001302554.2:c.211G>A NP_001289483.1:p.Val71Met