Canonical Allele Identifier: CA1621731030

Gene: TBC1D22B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37311024_37311025delinsAT , CM000668.2:g.37311024_37311025delinsAT	GRCh38
NC_000006.11:g.37278800_37278801delinsAT , CM000668.1:g.37278800_37278801delinsAT	GRCh37
NC_000006.10:g.37386778_37386779delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373491.3:c.983-1894_983-1893delinsAT MANE Select	ENSP00000362590.3:n.983-1894_983-1893delinsAT
NM_017772.3:c.983-1894_983-1893delinsAT	NP_060242.2:n.983-1894_983-1893delinsAT
NR_130108.1:n.1258-1894_1258-1893delinsAT
XM_011514738.1:c.983-1894_983-1893delinsAT	XP_011513040.1:n.983-1894_983-1893delinsAT
XM_011514739.1:c.983-1894_983-1893delinsAT	XP_011513041.1:n.983-1894_983-1893delinsAT
XR_241906.1:n.1034-1894_1034-1893delinsAT
XR_427833.1:n.1149-1856_1149-1855delinsAT
XR_926270.1:n.1149-1856_1149-1855delinsAT
XM_011514738.3:c.983-1894_983-1893delinsAT	XP_011513040.1:n.983-1894_983-1893delinsAT
XM_011514739.2:c.983-1894_983-1893delinsAT	XP_011513041.1:n.983-1894_983-1893delinsAT
XR_241906.2:n.1014-1894_1014-1893delinsAT
XR_427833.2:n.1129-1856_1129-1855delinsAT
XR_926270.3:n.1129-1856_1129-1855delinsAT
NM_017772.4:c.983-1894_983-1893delinsAT MANE Select	NP_060242.2:n.983-1894_983-1893delinsAT
NR_130108.2:n.1190-1894_1190-1893delinsAT