Canonical Allele Identifier: CA1483148903

Gene: TBCK

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.106235316G= , CM000666.2:g.106235316G=	GRCh38
NC_000004.11:g.107156473G= , CM000666.1:g.107156473G=	GRCh37
NC_000004.10:g.107375922G=	NCBI36
NG_034057.2:g.91180C=
NG_034057.3:g.86368C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273980.10:c.1402C=	ENSP00000273980.4:p.Pro468=
ENST00000394708.7:c.1402C= MANE Select	ENSP00000378198.2:p.Pro468=
ENST00000273980.9:c.1402C=	ENSP00000273980.4:p.Pro468=
ENST00000361687.8:c.1213C=	ENSP00000355338.4:p.Pro405=
ENST00000394706.7:c.1285C=	ENSP00000378196.3:p.Pro429=
ENST00000394708.6:c.1402C=	ENSP00000378198.2:p.Pro468=
ENST00000432496.6:c.1402C=	ENSP00000405847.2:p.Pro468=
ENST00000467183.6:c.*1041C=	ENSP00000421182.1:n.*1041C=
ENST00000503516.1:c.-9C=	ENSP00000423834.1:n.-9C=
ENST00000508666.5:c.666C=
ENST00000510927.5:n.1055C=
NM_001163435.2:c.1402C=	NP_001156907.1:p.Pro468=
NM_001163436.2:c.1402C=	NP_001156908.1:p.Pro468=
NM_001163437.2:c.1285C=	NP_001156909.1:p.Pro429=
NM_001290768.1:c.886C=	NP_001277697.1:p.Pro296=
NM_033115.4:c.1213C=	NP_149106.2:p.Pro405=
XM_006714419.2:c.1402C=	XP_006714482.1:p.Pro468=
XM_011532417.1:c.1402C=	XP_011530719.1:p.Pro468=
XM_011532418.1:c.1084C=	XP_011530720.1:p.Pro362=
XM_011532419.1:c.886C=	XP_011530721.1:p.Pro296=
XR_938800.1:n.1431C=
XM_011532417.2:c.1402C=	XP_011530719.1:p.Pro468=
XM_017008846.1:c.1402C=	XP_016864335.1:p.Pro468=
XM_017008847.2:c.1402C=	XP_016864336.1:p.Pro468=
XM_017008848.1:c.1084C=	XP_016864337.1:p.Pro362=
XM_017008849.1:c.886C=	XP_016864338.1:p.Pro296=
XM_024454281.1:c.1402C=	XP_024310049.1:p.Pro468=
XM_024454282.1:c.1402C=	XP_024310050.1:p.Pro468=
XR_001741353.2:n.1742C=
XR_001741354.2:n.1339C=
XR_002959772.1:n.1526C=
XR_938800.3:n.1742C=
NM_001163435.3:c.1402C= MANE Select	NP_001156907.2:p.Pro468=
NM_001163436.4:c.1402C=	NP_001156908.2:p.Pro468=
NM_001163437.3:c.1285C=	NP_001156909.2:p.Pro429=
NM_001290768.2:c.886C=	NP_001277697.2:p.Pro296=
NM_033115.5:c.1213C=	NP_149106.3:p.Pro405=