Canonical Allele Identifier: CA2574378789

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609721_54609733del , CM000663.2:g.54609721_54609733del	GRCh38
NC_000001.10:g.55075394_55075406del , CM000663.1:g.55075394_55075406del	GRCh37
NC_000001.9:g.54847982_54847994del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1296_1308del (FAM151A) MANE Select	ENSP00000306888.2:p.Ser433CysfsTer?
ENST00000343744.7:c.*609_*621del (ACOT11) MANE Select	ENSP00000340260.2:n.*609_*621del
ENST00000302250.6:c.1296_1308del (FAM151A)	ENSP00000306888.2:p.Ser433CysfsTer?
ENST00000343744.6:c.*609_*621del (ACOT11)	ENSP00000340260.2:n.*609_*621del
ENST00000371304.2:c.918-183_918-171del (FAM151A)	ENSP00000360353.2:n.918-183_918-171del
ENST00000371316.3:c.1629+1653_1629+1665del (ACOT11)	ENSP00000360366.3:n.1629+1653_1629+1665del
ENST00000481208.5:n.2472_2484del (ACOT11)
NM_015547.3:c.1629+1653_1629+1665del (ACOT11)	NP_056362.1:n.1629+1653_1629+1665del
NM_147161.3:c.*609_*621del (ACOT11)	NP_671517.1:n.*609_*621del
NM_176782.2:c.1296_1308del (FAM151A)	NP_788954.2:p.Ser433CysfsTer?
XM_006710599.2:c.1218_1230del (FAM151A)	XP_006710662.1:p.Ser407CysfsTer?
XM_006710599.3:c.1218_1230del (FAM151A)	XP_006710662.1:p.Ser407CysfsTer?
NM_176782.3:c.1296_1308del (FAM151A) MANE Select	NP_788954.2:p.Ser433CysfsTer?
NM_015547.4:c.1629+1653_1629+1665del (ACOT11)	NP_056362.1:n.1629+1653_1629+1665del
NM_147161.4:c.*609_*621del (ACOT11) MANE Select	NP_671517.1:n.*609_*621del