Canonical Allele Identifier: CA771638004

Gene: ACACA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37162308T>A , CM000679.2:g.37162308T>A	GRCh38
NG_023295.2:g.249504A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616317.5:c.5080-258A>T MANE Select	ENSP00000483300.1:n.5080-258A>T
ENST00000612895.4:c.4795-258A>T	ENSP00000482269.1:n.4795-258A>T
ENST00000614428.4:c.4969-258A>T	ENSP00000478547.1:n.4969-258A>T
ENST00000616317.4:c.5080-258A>T	ENSP00000483300.1:n.5080-258A>T
ENST00000617649.4:c.4735-258A>T	ENSP00000482368.1:n.4735-258A>T
ENST00000618575.1:n.322-258A>T
ENST00000619546.4:c.925-258A>T	ENSP00000483969.1:n.925-258A>T
NM_198834.2:c.5080-258A>T	NP_942131.1:n.5080-258A>T
NM_198836.2:c.4969-258A>T	NP_942133.1:n.4969-258A>T
NM_198837.1:c.4795-258A>T	NP_942134.1:n.4795-258A>T
NM_198838.1:c.4735-258A>T	NP_942135.1:n.4735-258A>T
NM_198839.2:c.4969-258A>T	NP_942136.1:n.4969-258A>T
XM_005257267.3:c.4735-258A>T	XP_005257324.1:n.4735-258A>T
XM_006721853.1:c.5056-258A>T	XP_006721916.1:n.5056-258A>T
XM_011524701.1:c.4990-258A>T	XP_011523003.1:n.4990-258A>T
XM_011524702.1:c.4969-258A>T	XP_011523004.1:n.4969-258A>T
XM_011524703.1:c.4969-258A>T	XP_011523005.1:n.4969-258A>T
XM_011524704.1:c.4735-258A>T	XP_011523006.1:n.4735-258A>T
XR_934449.1:n.5603-258A>T
XM_005257267.5:c.4735-258A>T	XP_005257324.1:n.4735-258A>T
XM_011524704.2:c.4735-258A>T	XP_011523006.1:n.4735-258A>T
XM_017024553.1:c.5104-258A>T	XP_016880042.1:n.5104-258A>T
XM_017024554.1:c.5080-258A>T	XP_016880043.1:n.5080-258A>T
XM_017024555.1:c.4969-258A>T	XP_016880044.1:n.4969-258A>T
XR_001752504.1:n.5627-258A>T
NM_198834.3:c.5080-258A>T MANE Select	NP_942131.1:n.5080-258A>T
NM_198836.3:c.4969-258A>T	NP_942133.1:n.4969-258A>T
NM_198837.2:c.4795-258A>T	NP_942134.1:n.4795-258A>T
NM_198838.2:c.4735-258A>T	NP_942135.1:n.4735-258A>T
NM_198839.3:c.4969-258A>T	NP_942136.1:n.4969-258A>T