Canonical Allele Identifier: CA1621731009

Gene: TBC1D22B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.37310979_37310981delinsAAC , CM000668.2:g.37310979_37310981delinsAAC	GRCh38
NC_000006.11:g.37278755_37278757delinsAAC , CM000668.1:g.37278755_37278757delinsAAC	GRCh37
NC_000006.10:g.37386733_37386735delinsAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373491.3:c.983-1939_983-1937delinsAAC MANE Select	ENSP00000362590.3:n.983-1939_983-1937delinsAAC
NM_017772.3:c.983-1939_983-1937delinsAAC	NP_060242.2:n.983-1939_983-1937delinsAAC
NR_130108.1:n.1258-1939_1258-1937delinsAAC
XM_011514738.1:c.983-1939_983-1937delinsAAC	XP_011513040.1:n.983-1939_983-1937delinsAAC
XM_011514739.1:c.983-1939_983-1937delinsAAC	XP_011513041.1:n.983-1939_983-1937delinsAAC
XR_241906.1:n.1034-1939_1034-1937delinsAAC
XR_427833.1:n.1149-1901_1149-1899delinsAAC
XR_926270.1:n.1149-1901_1149-1899delinsAAC
XM_011514738.3:c.983-1939_983-1937delinsAAC	XP_011513040.1:n.983-1939_983-1937delinsAAC
XM_011514739.2:c.983-1939_983-1937delinsAAC	XP_011513041.1:n.983-1939_983-1937delinsAAC
XR_241906.2:n.1014-1939_1014-1937delinsAAC
XR_427833.2:n.1129-1901_1129-1899delinsAAC
XR_926270.3:n.1129-1901_1129-1899delinsAAC
NM_017772.4:c.983-1939_983-1937delinsAAC MANE Select	NP_060242.2:n.983-1939_983-1937delinsAAC
NR_130108.2:n.1190-1939_1190-1937delinsAAC