Canonical Allele Identifier: CA340441034

Gene: FAM151A ACOT11

Linked Data

• gnomAD v4: 1-54609347-G-A
• MyVariant Identifiers: chr1:g.55075020G>A (hg19) ; chr1:g.54609347G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609347G>A , CM000663.2:g.54609347G>A	GRCh38
NC_000001.10:g.55075020G>A , CM000663.1:g.55075020G>A	GRCh37
NC_000001.9:g.54847608G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1679C>T (FAM151A) MANE Select	ENSP00000306888.2:p.Ala560Val
ENST00000343744.7:c.*235G>A (ACOT11) MANE Select	ENSP00000340260.2:n.*235G>A
ENST00000302250.6:c.1679C>T (FAM151A)	ENSP00000306888.2:p.Ala560Val
ENST00000343744.6:c.*235G>A (ACOT11)	ENSP00000340260.2:n.*235G>A
ENST00000371304.2:c.1118C>T (FAM151A)	ENSP00000360353.2:p.Ala373Val
ENST00000371316.3:c.1629+1279G>A (ACOT11)	ENSP00000360366.3:n.1629+1279G>A
ENST00000481208.5:n.2098G>A (ACOT11)
NM_015547.3:c.1629+1279G>A (ACOT11)	NP_056362.1:n.1629+1279G>A
NM_147161.3:c.*235G>A (ACOT11)	NP_671517.1:n.*235G>A
NM_176782.2:c.1679C>T (FAM151A)	NP_788954.2:p.Ala560Val
XM_006710599.2:c.1601C>T (FAM151A)	XP_006710662.1:p.Ala534Val
XM_006710599.3:c.1601C>T (FAM151A)	XP_006710662.1:p.Ala534Val
NM_176782.3:c.1679C>T (FAM151A) MANE Select	NP_788954.2:p.Ala560Val
NM_015547.4:c.1629+1279G>A (ACOT11)	NP_056362.1:n.1629+1279G>A
NM_147161.4:c.*235G>A (ACOT11) MANE Select	NP_671517.1:n.*235G>A