Canonical Allele Identifier: CA340441061

Gene: FAM151A ACOT11

Linked Data

• dbSNP Id: rs1238032153
• gnomAD v2: 1-55075026-G-A
• gnomAD v4: 1-54609353-G-A
• MyVariant Identifiers: chr1:g.55075026G>A (hg19) ; chr1:g.54609353G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609353G>A , CM000663.2:g.54609353G>A	GRCh38
NC_000001.10:g.55075026G>A , CM000663.1:g.55075026G>A	GRCh37
NC_000001.9:g.54847614G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1673C>T (FAM151A) MANE Select	ENSP00000306888.2:p.Ala558Val
ENST00000343744.7:c.*241G>A (ACOT11) MANE Select	ENSP00000340260.2:n.*241G>A
ENST00000302250.6:c.1673C>T (FAM151A)	ENSP00000306888.2:p.Ala558Val
ENST00000343744.6:c.*241G>A (ACOT11)	ENSP00000340260.2:n.*241G>A
ENST00000371304.2:c.1112C>T (FAM151A)	ENSP00000360353.2:p.Ala371Val
ENST00000371316.3:c.1629+1285G>A (ACOT11)	ENSP00000360366.3:n.1629+1285G>A
ENST00000481208.5:n.2104G>A (ACOT11)
NM_015547.3:c.1629+1285G>A (ACOT11)	NP_056362.1:n.1629+1285G>A
NM_147161.3:c.*241G>A (ACOT11)	NP_671517.1:n.*241G>A
NM_176782.2:c.1673C>T (FAM151A)	NP_788954.2:p.Ala558Val
XM_006710599.2:c.1595C>T (FAM151A)	XP_006710662.1:p.Ala532Val
XM_006710599.3:c.1595C>T (FAM151A)	XP_006710662.1:p.Ala532Val
NM_176782.3:c.1673C>T (FAM151A) MANE Select	NP_788954.2:p.Ala558Val
NM_015547.4:c.1629+1285G>A (ACOT11)	NP_056362.1:n.1629+1285G>A
NM_147161.4:c.*241G>A (ACOT11) MANE Select	NP_671517.1:n.*241G>A