Canonical Allele Identifier: CA103420309

Gene: TBCK

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.106294917_106294918del , CM000666.2:g.106294917_106294918del	GRCh38
NC_000004.11:g.107216074_107216075del , CM000666.1:g.107216074_107216075del	GRCh37
NC_000004.10:g.107435523_107435524del	NCBI36
NG_034057.2:g.31579_31580del
NG_034057.3:g.26767_26768del

Transcript Alleles

HGVS	Amino-acid Change
NM_001163435.3:c.266+177_266+178del MANE Select	NP_001156907.2:n.266+177_266+178del
ENST00000394708.7:c.266+177_266+178del MANE Select	ENSP00000378198.2:n.266+177_266+178del
NM_001163435.2:c.266+177_266+178del	NP_001156907.1:n.266+177_266+178del
NM_001163436.2:c.266+177_266+178del	NP_001156908.1:n.266+177_266+178del
NM_001163436.4:c.266+177_266+178del	NP_001156908.2:n.266+177_266+178del
NM_001163437.2:c.266+177_266+178del	NP_001156909.1:n.266+177_266+178del
NM_001163437.3:c.266+177_266+178del	NP_001156909.2:n.266+177_266+178del
NM_001290768.1:c.-352+177_-352+178del	NP_001277697.1:n.-352+177_-352+178del
NM_001290768.2:c.-352+177_-352+178del	NP_001277697.2:n.-352+177_-352+178del
NM_033115.4:c.266+177_266+178del	NP_149106.2:n.266+177_266+178del
NM_033115.5:c.266+177_266+178del	NP_149106.3:n.266+177_266+178del
ENST00000273980.10:c.266+177_266+178del	ENSP00000273980.4:n.266+177_266+178del
ENST00000273980.9:c.266+177_266+178del	ENSP00000273980.4:n.266+177_266+178del
ENST00000361687.8:c.266+177_266+178del	ENSP00000355338.4:n.266+177_266+178del
ENST00000394706.7:c.266+177_266+178del	ENSP00000378196.3:n.266+177_266+178del
ENST00000394708.6:c.266+177_266+178del	ENSP00000378198.2:n.266+177_266+178del
ENST00000432496.6:c.266+177_266+178del	ENSP00000405847.2:n.266+177_266+178del
ENST00000467183.6:c.266+177_266+178del	ENSP00000421182.1:n.266+177_266+178del
ENST00000506280.1:n.101+177_101+178del
ENST00000509532.5:c.266+177_266+178del	ENSP00000420985.1:n.266+177_266+178del
ENST00000509862.5:c.266+177_266+178del	ENSP00000425197.1:n.266+177_266+178del
XM_006714419.2:c.266+177_266+178del	XP_006714482.1:n.266+177_266+178del
XM_011532417.1:c.266+177_266+178del	XP_011530719.1:n.266+177_266+178del
XM_011532417.2:c.266+177_266+178del	XP_011530719.1:n.266+177_266+178del
XM_011532418.1:c.-53+177_-53+178del	XP_011530720.1:n.-53+177_-53+178del
XM_011532419.1:c.-62+177_-62+178del	XP_011530721.1:n.-62+177_-62+178del
XM_017008846.1:c.266+177_266+178del	XP_016864335.1:n.266+177_266+178del
XM_017008847.2:c.266+177_266+178del	XP_016864336.1:n.266+177_266+178del
XM_017008848.1:c.-53+177_-53+178del	XP_016864337.1:n.-53+177_-53+178del
XM_017008849.1:c.-62+177_-62+178del	XP_016864338.1:n.-62+177_-62+178del
XM_024454281.1:c.266+177_266+178del	XP_024310049.1:n.266+177_266+178del
XM_024454282.1:c.266+177_266+178del	XP_024310050.1:n.266+177_266+178del
XR_001741353.2:n.606+177_606+178del
XR_001741354.2:n.203+177_203+178del
XR_938800.1:n.295+177_295+178del
XR_938800.3:n.606+177_606+178del
XR_939042.1:n.469-1173_469-1172del
XR_939043.1:n.432-1173_432-1172del
XR_939044.1:n.353-1173_353-1172del