Canonical Allele Identifier: CA1167798524

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609533_54609535delinsAGC , CM000663.2:g.54609533_54609535delinsAGC	GRCh38
NC_000001.10:g.55075206_55075208delinsAGC , CM000663.1:g.55075206_55075208delinsAGC	GRCh37
NC_000001.9:g.54847794_54847796delinsAGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1491_1493delinsGCT (FAM151A) MANE Select	ENSP00000306888.2:p.Met497=
ENST00000343744.7:c.*421_*423delinsAGC (ACOT11) MANE Select	ENSP00000340260.2:n.*421_*423delinsAGC
ENST00000302250.6:c.1491_1493delinsGCT (FAM151A)	ENSP00000306888.2:p.Met497=
ENST00000343744.6:c.*421_*423delinsAGC (ACOT11)	ENSP00000340260.2:n.*421_*423delinsAGC
ENST00000371304.2:c.930_932delinsGCT (FAM151A)	ENSP00000360353.2:p.Met310=
ENST00000371316.3:c.1629+1465_1629+1467delinsAGC (ACOT11)	ENSP00000360366.3:n.1629+1465_1629+1467delinsAGC
ENST00000481208.5:n.2284_2286delinsAGC (ACOT11)
NM_015547.3:c.1629+1465_1629+1467delinsAGC (ACOT11)	NP_056362.1:n.1629+1465_1629+1467delinsAGC
NM_147161.3:c.*421_*423delinsAGC (ACOT11)	NP_671517.1:n.*421_*423delinsAGC
NM_176782.2:c.1491_1493delinsGCT (FAM151A)	NP_788954.2:p.Met497=
XM_006710599.2:c.1413_1415delinsGCT (FAM151A)	XP_006710662.1:p.Met471=
XM_006710599.3:c.1413_1415delinsGCT (FAM151A)	XP_006710662.1:p.Met471=
NM_176782.3:c.1491_1493delinsGCT (FAM151A) MANE Select	NP_788954.2:p.Met497=
NM_015547.4:c.1629+1465_1629+1467delinsAGC (ACOT11)	NP_056362.1:n.1629+1465_1629+1467delinsAGC
NM_147161.4:c.*421_*423delinsAGC (ACOT11) MANE Select	NP_671517.1:n.*421_*423delinsAGC