Canonical Allele Identifier: CA916179746

Gene: FAM151A ACOT11

Linked Data

• dbSNP Id: rs1557668114
• gnomAD v4: 1-54609603-TCACGTGGGGGAAGACCTCAGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609607_54609627del , CM000663.2:g.54609607_54609627del	GRCh38
NC_000001.10:g.55075280_55075300del , CM000663.1:g.55075280_55075300del	GRCh37
NC_000001.9:g.54847868_54847888del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1402_1422del (FAM151A) MANE Select	ENSP00000306888.2:p.Ala468_Val474del
ENST00000343744.7:c.*495_*515del (ACOT11) MANE Select	ENSP00000340260.2:n.*495_*515del
ENST00000302250.6:c.1402_1422del (FAM151A)	ENSP00000306888.2:p.Ala468_Val474del
ENST00000343744.6:c.*495_*515del (ACOT11)	ENSP00000340260.2:n.*495_*515del
ENST00000371304.2:c.918-77_918-57del (FAM151A)	ENSP00000360353.2:n.918-77_918-57del
ENST00000371316.3:c.1629+1539_1629+1559del (ACOT11)	ENSP00000360366.3:n.1629+1539_1629+1559del
ENST00000481208.5:n.2358_2378del (ACOT11)
NM_015547.3:c.1629+1539_1629+1559del (ACOT11)	NP_056362.1:n.1629+1539_1629+1559del
NM_147161.3:c.*495_*515del (ACOT11)	NP_671517.1:n.*495_*515del
NM_176782.2:c.1402_1422del (FAM151A)	NP_788954.2:p.Ala468_Val474del
XM_006710599.2:c.1324_1344del (FAM151A)	XP_006710662.1:p.Ala442_Val448del
XM_006710599.3:c.1324_1344del (FAM151A)	XP_006710662.1:p.Ala442_Val448del
NM_176782.3:c.1402_1422del (FAM151A) MANE Select	NP_788954.2:p.Ala468_Val474del
NM_015547.4:c.1629+1539_1629+1559del (ACOT11)	NP_056362.1:n.1629+1539_1629+1559del
NM_147161.4:c.*495_*515del (ACOT11) MANE Select	NP_671517.1:n.*495_*515del