Canonical Allele Identifier: CA1167798380

Gene: FAM151A ACOT11

Linked Data

• dbSNP Id: rs1644079033

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609231_54609237del , CM000663.2:g.54609231_54609237del	GRCh38
NC_000001.10:g.55074904_55074910del , CM000663.1:g.55074904_55074910del	GRCh37
NC_000001.9:g.54847492_54847498del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.*34_*40del (FAM151A) MANE Select	ENSP00000306888.2:n.*34_*40del
ENST00000343744.7:c.*119_*125del (ACOT11) MANE Select	ENSP00000340260.2:n.*119_*125del
ENST00000302250.6:c.*34_*40del (FAM151A)	ENSP00000306888.2:n.*34_*40del
ENST00000343744.6:c.*119_*125del (ACOT11)	ENSP00000340260.2:n.*119_*125del
ENST00000371304.2:c.*34_*40del (FAM151A)	ENSP00000360353.2:n.*34_*40del
ENST00000371316.3:c.1629+1163_1629+1169del (ACOT11)	ENSP00000360366.3:n.1629+1163_1629+1169del
ENST00000481208.5:n.1982_1988del (ACOT11)
NM_015547.3:c.1629+1163_1629+1169del (ACOT11)	NP_056362.1:n.1629+1163_1629+1169del
NM_147161.3:c.*119_*125del (ACOT11)	NP_671517.1:n.*119_*125del
NM_176782.2:c.*34_*40del (FAM151A)	NP_788954.2:n.*34_*40del
XM_006710599.2:c.*34_*40del (FAM151A)	XP_006710662.1:n.*34_*40del
XM_006710599.3:c.*34_*40del (FAM151A)	XP_006710662.1:n.*34_*40del
NM_176782.3:c.*34_*40del (FAM151A) MANE Select	NP_788954.2:n.*34_*40del
NM_015547.4:c.1629+1163_1629+1169del (ACOT11)	NP_056362.1:n.1629+1163_1629+1169del
NM_147161.4:c.*119_*125del (ACOT11) MANE Select	NP_671517.1:n.*119_*125del