Canonical Allele Identifier: CA243649042

Gene: ACAD10

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111730205G>A , CM000674.2:g.111730205G>A	GRCh38
NC_000012.11:g.112168009G>A , CM000674.1:g.112168009G>A	GRCh37
NC_000012.10:g.110652392G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313698.9:c.1394+249G>A MANE Select	ENSP00000325137.5:n.1394+249G>A
ENST00000313698.8:c.1394+249G>A	ENSP00000325137.4:n.1394+249G>A
ENST00000413681.7:n.1579+249G>A
ENST00000455480.6:c.1487+249G>A	ENSP00000389813.2:n.1487+249G>A
ENST00000507683.1:c.527+2062G>A
ENST00000508303.5:n.544+249G>A
ENST00000515283.1:c.-107-14438G>A	ENSP00000449097.1:n.-107-14438G>A
ENST00000549590.5:c.1394+249G>A	ENSP00000446959.1:n.1394+249G>A
ENST00000552706.6:c.553+2062G>A	ENSP00000447561.2:n.553+2062G>A
NM_001136538.1:c.1487+249G>A	NP_001130010.1:n.1487+249G>A
NM_025247.5:c.1394+249G>A	NP_079523.3:n.1394+249G>A
NM_001136538.2:c.1487+249G>A	NP_001130010.1:n.1487+249G>A
NM_025247.6:c.1394+249G>A MANE Select	NP_079523.3:n.1394+249G>A