Canonical Allele Identifier: CA866936

Gene: FAM151A ACOT11

Linked Data

• dbSNP Id: rs761738488
• ExAC: 1:55075394 G / T
• gnomAD v2: 1-55075394-G-T
• gnomAD v4: 1-54609721-G-T
• MyVariant Identifiers: chr1:g.55075394G>T (hg19) ; chr1:g.54609721G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609721G>T , CM000663.2:g.54609721G>T	GRCh38
NC_000001.10:g.55075394G>T , CM000663.1:g.55075394G>T	GRCh37
NC_000001.9:g.54847982G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1305C>A (FAM151A) MANE Select	ENSP00000306888.2:p.Gly435=
ENST00000343744.7:c.*609G>T (ACOT11) MANE Select	ENSP00000340260.2:n.*609G>T
ENST00000302250.6:c.1305C>A (FAM151A)	ENSP00000306888.2:p.Gly435=
ENST00000343744.6:c.*609G>T (ACOT11)	ENSP00000340260.2:n.*609G>T
ENST00000371304.2:c.918-174C>A (FAM151A)	ENSP00000360353.2:n.918-174C>A
ENST00000371316.3:c.1629+1653G>T (ACOT11)	ENSP00000360366.3:n.1629+1653G>T
ENST00000481208.5:n.2472G>T (ACOT11)
NM_015547.3:c.1629+1653G>T (ACOT11)	NP_056362.1:n.1629+1653G>T
NM_147161.3:c.*609G>T (ACOT11)	NP_671517.1:n.*609G>T
NM_176782.2:c.1305C>A (FAM151A)	NP_788954.2:p.Gly435=
XM_006710599.2:c.1227C>A (FAM151A)	XP_006710662.1:p.Gly409=
XM_006710599.3:c.1227C>A (FAM151A)	XP_006710662.1:p.Gly409=
NM_176782.3:c.1305C>A (FAM151A) MANE Select	NP_788954.2:p.Gly435=
NM_015547.4:c.1629+1653G>T (ACOT11)	NP_056362.1:n.1629+1653G>T
NM_147161.4:c.*609G>T (ACOT11) MANE Select	NP_671517.1:n.*609G>T