Canonical Allele Identifier: CA684415973
Gene: ACADS HGNC NCBI

Linked Data

dbSNP Id: rs1267786315

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.120736848_120736856dup , CM000674.2:g.120736848_120736856dup GRCh38
NC_000012.11:g.121174651_121174659dup , CM000674.1:g.121174651_121174659dup GRCh37
NC_000012.10:g.119659034_119659042dup NCBI36
NG_007991.1:g.16081_16089dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000242592.9:c.211-138_211-130dup MANE Select ENSP00000242592.4:n.211-138_211-130dup
ENST00000242592.8:c.211-138_211-130dup ENSP00000242592.4:n.211-138_211-130dup
ENST00000411593.2:c.211-138_211-130dup ENSP00000401045.2:n.211-138_211-130dup
ENST00000539690.1:n.323-138_323-130dup
NM_000017.3:c.211-138_211-130dup NP_000008.1:n.211-138_211-130dup
NM_001302554.1:c.211-138_211-130dup NP_001289483.1:n.211-138_211-130dup
NM_000017.4:c.211-138_211-130dup MANE Select NP_000008.1:n.211-138_211-130dup
NM_001302554.2:c.211-138_211-130dup NP_001289483.1:n.211-138_211-130dup