Canonical Allele Identifier: CA2167575942

Gene: GOLGA8H DNM1P50 ARHGAP11B-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.30606145G= , CM000677.2:g.30606145G=	GRCh38
NC_000015.9:g.30898348G= , CM000677.1:g.30898348G=	GRCh37
NC_000015.8:g.28685640G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000566740.2:c.168+183G= (GOLGA8H) MANE Select	ENSP00000456894.1:n.168+183G=
ENST00000566740.1:c.168+183G= (GOLGA8H)	ENSP00000456894.1:n.168+183G=
NM_001282490.1:c.168+183G= (GOLGA8H)	NP_001269419.1:n.168+183G=
XM_006720672.2:c.129+183G= (GOLGA8H)	XP_006720735.1:n.129+183G=
XM_011521990.1:c.-286+183G= (GOLGA8H)	XP_011520292.1:n.-286+183G=
XM_011522274.1:c.-308+2073C= (DNM1P50)	XP_011520576.1:n.-308+2073C=
XM_011522275.1:c.-308+2073C= (DNM1P50)	XP_011520577.1:n.-308+2073C=
XM_011522276.1:c.-308+2073C= (DNM1P50)	XP_011520578.1:n.-308+2073C=
XM_011522278.1:c.-308+2073C= (DNM1P50)	XP_011520580.1:n.-308+2073C=
XM_011522282.1:c.209+2073C= (DNM1P50)	XP_011520584.1:n.209+2073C=
XM_011522283.1:c.209+2073C= (DNM1P50)	XP_011520585.1:n.209+2073C=
XR_932037.1:n.1044+2073C= (DNM1P50)
XR_932039.1:n.1166+2073C= (DNM1P50)
XR_932042.1:n.786+2073C= (DNM1P50)
XR_932043.1:n.707+18906C= (DNM1P50)
XR_932044.1:n.708-11853C= (DNM1P50)
XR_932045.1:n.707+18906C= (DNM1P50)
NR_157593.1:n.851-11853C= (ARHGAP11B-DT)
NR_157594.1:n.849+2073C= (ARHGAP11B-DT)
NR_157595.1:n.513-11853C= (ARHGAP11B-DT)
NM_001282490.2:c.168+183G= (GOLGA8H) MANE Select	NP_001269419.1:n.168+183G=