Canonical Allele Identifier: CA2621365473

Gene: ACADS

Linked Data

• gnomAD v4: 12-120736917-T-TTTGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120736923_120736928dup , CM000674.2:g.120736923_120736928dup	GRCh38
NC_000012.11:g.121174726_121174731dup , CM000674.1:g.121174726_121174731dup	GRCh37
NC_000012.10:g.119659109_119659114dup	NCBI36
NG_007991.1:g.16156_16161dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000242592.9:c.211-63_211-58dup MANE Select	ENSP00000242592.4:n.211-63_211-58dup
ENST00000242592.8:c.211-63_211-58dup	ENSP00000242592.4:n.211-63_211-58dup
ENST00000411593.2:c.211-63_211-58dup	ENSP00000401045.2:n.211-63_211-58dup
ENST00000539690.1:n.323-63_323-58dup
NM_000017.3:c.211-63_211-58dup	NP_000008.1:n.211-63_211-58dup
NM_001302554.1:c.211-63_211-58dup	NP_001289483.1:n.211-63_211-58dup
NM_000017.4:c.211-63_211-58dup MANE Select	NP_000008.1:n.211-63_211-58dup
NM_001302554.2:c.211-63_211-58dup	NP_001289483.1:n.211-63_211-58dup