Canonical Allele Identifier: CA771621616

Gene: ACACA

Linked Data

• dbSNP Id: rs1173776000
• gnomAD v3: 17-37111054-G-C
• gnomAD v4: 17-37111054-G-C
• MyVariant Identifiers: chr17:g.37111054G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.37111054G>C , CM000679.2:g.37111054G>C	GRCh38
NC_000017.10:g.35467989G>C , CM000679.1:g.35467989G>C	GRCh37
NC_000017.9:g.32542102G>C	NCBI36
NG_023295.2:g.300758C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616317.5:c.6565+477C>G MANE Select	ENSP00000483300.1:n.6565+477C>G
ENST00000612895.4:c.6280+477C>G	ENSP00000482269.1:n.6280+477C>G
ENST00000613776.1:n.691+477C>G
ENST00000614428.4:c.6454+477C>G	ENSP00000478547.1:n.6454+477C>G
ENST00000614482.4:c.1150+477C>G
ENST00000616317.4:c.6565+477C>G	ENSP00000483300.1:n.6565+477C>G
ENST00000617649.4:c.6220+477C>G	ENSP00000482368.1:n.6220+477C>G
ENST00000619546.4:c.2410+477C>G	ENSP00000483969.1:n.2410+477C>G
NM_198834.2:c.6565+477C>G	NP_942131.1:n.6565+477C>G
NM_198836.2:c.6454+477C>G	NP_942133.1:n.6454+477C>G
NM_198837.1:c.6280+477C>G	NP_942134.1:n.6280+477C>G
NM_198838.1:c.6220+477C>G	NP_942135.1:n.6220+477C>G
NM_198839.2:c.6454+477C>G	NP_942136.1:n.6454+477C>G
XM_005257267.3:c.6220+477C>G	XP_005257324.1:n.6220+477C>G
XM_006721853.1:c.6541+477C>G	XP_006721916.1:n.6541+477C>G
XM_011524701.1:c.6475+477C>G	XP_011523003.1:n.6475+477C>G
XM_011524702.1:c.6454+477C>G	XP_011523004.1:n.6454+477C>G
XM_011524703.1:c.6454+477C>G	XP_011523005.1:n.6454+477C>G
XM_011524704.1:c.6220+477C>G	XP_011523006.1:n.6220+477C>G
XM_005257267.5:c.6220+477C>G	XP_005257324.1:n.6220+477C>G
XM_011524704.2:c.6220+477C>G	XP_011523006.1:n.6220+477C>G
XM_017024553.1:c.6589+477C>G	XP_016880042.1:n.6589+477C>G
XM_017024554.1:c.6565+477C>G	XP_016880043.1:n.6565+477C>G
XM_017024555.1:c.6454+477C>G	XP_016880044.1:n.6454+477C>G
NM_198834.3:c.6565+477C>G MANE Select	NP_942131.1:n.6565+477C>G
NM_198836.3:c.6454+477C>G	NP_942133.1:n.6454+477C>G
NM_198837.2:c.6280+477C>G	NP_942134.1:n.6280+477C>G
NM_198838.2:c.6220+477C>G	NP_942135.1:n.6220+477C>G
NM_198839.3:c.6454+477C>G	NP_942136.1:n.6454+477C>G