Canonical Allele Identifier: CA2621369650

Gene: ACADS

Linked Data

• gnomAD v4: 12-120738954-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120738954G>C , CM000674.2:g.120738954G>C	GRCh38
NC_000012.11:g.121176757G>C , CM000674.1:g.121176757G>C	GRCh37
NC_000012.10:g.119661140G>C	NCBI36
NG_007991.1:g.18187G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000242592.9:c.1029+39G>C MANE Select	ENSP00000242592.4:n.1029+39G>C
ENST00000242592.8:c.1029+39G>C	ENSP00000242592.4:n.1029+39G>C
ENST00000411593.2:c.1017+39G>C	ENSP00000401045.2:n.1017+39G>C
NM_000017.3:c.1029+39G>C	NP_000008.1:n.1029+39G>C
NM_001302554.1:c.1017+39G>C	NP_001289483.1:n.1017+39G>C
NM_000017.4:c.1029+39G>C MANE Select	NP_000008.1:n.1029+39G>C
NM_001302554.2:c.1017+39G>C	NP_001289483.1:n.1017+39G>C