Canonical Allele Identifier: CA2621369737

Gene: ACADS

Linked Data

• gnomAD v4: 12-120738986-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.120738990_120738991del , CM000674.2:g.120738990_120738991del	GRCh38
NC_000012.11:g.121176793_121176794del , CM000674.1:g.121176793_121176794del	GRCh37
NC_000012.10:g.119661176_119661177del	NCBI36
NG_007991.1:g.18223_18224del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242592.9:c.1029+75_1029+76del MANE Select	ENSP00000242592.4:n.1029+75_1029+76del
ENST00000242592.8:c.1029+75_1029+76del	ENSP00000242592.4:n.1029+75_1029+76del
ENST00000411593.2:c.1017+75_1017+76del	ENSP00000401045.2:n.1017+75_1017+76del
NM_000017.3:c.1029+75_1029+76del	NP_000008.1:n.1029+75_1029+76del
NM_001302554.1:c.1017+75_1017+76del	NP_001289483.1:n.1017+75_1017+76del
NM_000017.4:c.1029+75_1029+76del MANE Select	NP_000008.1:n.1029+75_1029+76del
NM_001302554.2:c.1017+75_1017+76del	NP_001289483.1:n.1017+75_1017+76del