Canonical Allele Identifier: CA2645794434

Gene: FAM151A ACOT11

Linked Data

• gnomAD v4: 1-54609215-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609215T>G , CM000663.2:g.54609215T>G	GRCh38
NC_000001.10:g.55074888T>G , CM000663.1:g.55074888T>G	GRCh37
NC_000001.9:g.54847476T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*53A>C (FAM151A) MANE Select	ENSP00000306888.2:n.*53A>C
ENST00000343744.7:c.*103T>G (ACOT11) MANE Select	ENSP00000340260.2:n.*103T>G
ENST00000302250.6:c.*53A>C (FAM151A)	ENSP00000306888.2:n.*53A>C
ENST00000343744.6:c.*103T>G (ACOT11)	ENSP00000340260.2:n.*103T>G
ENST00000371304.2:c.*53A>C (FAM151A)	ENSP00000360353.2:n.*53A>C
ENST00000371316.3:c.1629+1147T>G (ACOT11)	ENSP00000360366.3:n.1629+1147T>G
ENST00000481208.5:n.1966T>G (ACOT11)
NM_015547.3:c.1629+1147T>G (ACOT11)	NP_056362.1:n.1629+1147T>G
NM_147161.3:c.*103T>G (ACOT11)	NP_671517.1:n.*103T>G
NM_176782.2:c.*53A>C (FAM151A)	NP_788954.2:n.*53A>C
XM_006710599.2:c.*53A>C (FAM151A)	XP_006710662.1:n.*53A>C
XM_006710599.3:c.*53A>C (FAM151A)	XP_006710662.1:n.*53A>C
NM_176782.3:c.*53A>C (FAM151A) MANE Select	NP_788954.2:n.*53A>C
NM_015547.4:c.1629+1147T>G (ACOT11)	NP_056362.1:n.1629+1147T>G
NM_147161.4:c.*103T>G (ACOT11) MANE Select	NP_671517.1:n.*103T>G