Canonical Allele Identifier: CA1621731034

Gene: TBC1D22B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37311032_37311034delinsCCT , CM000668.2:g.37311032_37311034delinsCCT	GRCh38
NC_000006.11:g.37278808_37278810delinsCCT , CM000668.1:g.37278808_37278810delinsCCT	GRCh37
NC_000006.10:g.37386786_37386788delinsCCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373491.3:c.983-1886_983-1884delinsCCT MANE Select	ENSP00000362590.3:n.983-1886_983-1884delinsCCT
NM_017772.3:c.983-1886_983-1884delinsCCT	NP_060242.2:n.983-1886_983-1884delinsCCT
NR_130108.1:n.1258-1886_1258-1884delinsCCT
XM_011514738.1:c.983-1886_983-1884delinsCCT	XP_011513040.1:n.983-1886_983-1884delinsCCT
XM_011514739.1:c.983-1886_983-1884delinsCCT	XP_011513041.1:n.983-1886_983-1884delinsCCT
XR_241906.1:n.1034-1886_1034-1884delinsCCT
XR_427833.1:n.1149-1848_1149-1846delinsCCT
XR_926270.1:n.1149-1848_1149-1846delinsCCT
XM_011514738.3:c.983-1886_983-1884delinsCCT	XP_011513040.1:n.983-1886_983-1884delinsCCT
XM_011514739.2:c.983-1886_983-1884delinsCCT	XP_011513041.1:n.983-1886_983-1884delinsCCT
XR_241906.2:n.1014-1886_1014-1884delinsCCT
XR_427833.2:n.1129-1848_1129-1846delinsCCT
XR_926270.3:n.1129-1848_1129-1846delinsCCT
NM_017772.4:c.983-1886_983-1884delinsCCT MANE Select	NP_060242.2:n.983-1886_983-1884delinsCCT
NR_130108.2:n.1190-1886_1190-1884delinsCCT