Canonical Allele Identifier: CA418177296

Gene: FAM151A ACOT11

Linked Data

• gnomAD v4: 1-54609394-A-C
• MyVariant Identifiers: chr1:g.55075067A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609394A>C , CM000663.2:g.54609394A>C	GRCh38
NC_000001.10:g.55075067A>C , CM000663.1:g.55075067A>C	GRCh37
NC_000001.9:g.54847655A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000302250.7:c.1632T>G (FAM151A) MANE Select	ENSP00000306888.2:p.Ala544=
ENST00000343744.7:c.*282A>C (ACOT11) MANE Select	ENSP00000340260.2:n.*282A>C
ENST00000302250.6:c.1632T>G (FAM151A)	ENSP00000306888.2:p.Ala544=
ENST00000343744.6:c.*282A>C (ACOT11)	ENSP00000340260.2:n.*282A>C
ENST00000371304.2:c.1071T>G (FAM151A)	ENSP00000360353.2:p.Ala357=
ENST00000371316.3:c.1629+1326A>C (ACOT11)	ENSP00000360366.3:n.1629+1326A>C
ENST00000481208.5:n.2145A>C (ACOT11)
NM_015547.3:c.1629+1326A>C (ACOT11)	NP_056362.1:n.1629+1326A>C
NM_147161.3:c.*282A>C (ACOT11)	NP_671517.1:n.*282A>C
NM_176782.2:c.1632T>G (FAM151A)	NP_788954.2:p.Ala544=
XM_006710599.2:c.1554T>G (FAM151A)	XP_006710662.1:p.Ala518=
XM_006710599.3:c.1554T>G (FAM151A)	XP_006710662.1:p.Ala518=
NM_176782.3:c.1632T>G (FAM151A) MANE Select	NP_788954.2:p.Ala544=
NM_015547.4:c.1629+1326A>C (ACOT11)	NP_056362.1:n.1629+1326A>C
NM_147161.4:c.*282A>C (ACOT11) MANE Select	NP_671517.1:n.*282A>C