Canonical Allele Identifier: CA1167798620

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609729_54609730delinsTG , CM000663.2:g.54609729_54609730delinsTG	GRCh38
NC_000001.10:g.55075402_55075403delinsTG , CM000663.1:g.55075402_55075403delinsTG	GRCh37
NC_000001.9:g.54847990_54847991delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1296_1297delinsCA (FAM151A) MANE Select	ENSP00000306888.2:p.Ser432=
ENST00000343744.7:c.*617_*618delinsTG (ACOT11) MANE Select	ENSP00000340260.2:n.*617_*618delinsTG
ENST00000302250.6:c.1296_1297delinsCA (FAM151A)	ENSP00000306888.2:p.Ser432=
ENST00000343744.6:c.*617_*618delinsTG (ACOT11)	ENSP00000340260.2:n.*617_*618delinsTG
ENST00000371304.2:c.918-183_918-182delinsCA (FAM151A)	ENSP00000360353.2:n.918-183_918-182delinsCA
ENST00000371316.3:c.1629+1661_1629+1662delinsTG (ACOT11)	ENSP00000360366.3:n.1629+1661_1629+1662delinsTG
ENST00000481208.5:n.2480_2481delinsTG (ACOT11)
NM_015547.3:c.1629+1661_1629+1662delinsTG (ACOT11)	NP_056362.1:n.1629+1661_1629+1662delinsTG
NM_147161.3:c.*617_*618delinsTG (ACOT11)	NP_671517.1:n.*617_*618delinsTG
NM_176782.2:c.1296_1297delinsCA (FAM151A)	NP_788954.2:p.Ser432=
XM_006710599.2:c.1218_1219delinsCA (FAM151A)	XP_006710662.1:p.Ser406=
XM_006710599.3:c.1218_1219delinsCA (FAM151A)	XP_006710662.1:p.Ser406=
NM_176782.3:c.1296_1297delinsCA (FAM151A) MANE Select	NP_788954.2:p.Ser432=
NM_015547.4:c.1629+1661_1629+1662delinsTG (ACOT11)	NP_056362.1:n.1629+1661_1629+1662delinsTG
NM_147161.4:c.*617_*618delinsTG (ACOT11) MANE Select	NP_671517.1:n.*617_*618delinsTG