Canonical Allele Identifier: CA407944664

Gene: TBC1D20

Linked Data

• dbSNP Id: rs2017204668
• MyVariant Identifiers: chr20:g.420992G>A (hg19) ; chr20:g.440348G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.440348G>A , CM000682.2:g.440348G>A	GRCh38
NC_000020.10:g.420992G>A , CM000682.1:g.420992G>A	GRCh37
NC_000020.9:g.368992G>A	NCBI36
NG_034082.1:g.27206C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354200.5:c.668C>T MANE Select	ENSP00000346139.4:p.Thr223Ile
ENST00000461188.6:n.1908C>T
ENST00000679451.1:n.893-31C>T
ENST00000679741.1:c.668C>T	ENSP00000504904.1:p.Thr223Ile
ENST00000679895.1:c.764C>T	ENSP00000505197.1:p.Thr255Ile
ENST00000679944.1:c.668C>T	ENSP00000506278.1:p.Thr223Ile
ENST00000679953.1:n.1557C>T
ENST00000679973.1:c.627-31C>T	ENSP00000506502.1:n.627-31C>T
ENST00000680050.1:c.482C>T	ENSP00000505464.1:p.Thr161Ile
ENST00000680088.1:n.813C>T
ENST00000680106.1:c.668C>T	ENSP00000505500.1:p.Thr223Ile
ENST00000680284.1:c.668C>T	ENSP00000506231.1:p.Thr223Ile
ENST00000680491.1:n.2159C>T
ENST00000680515.1:c.482C>T	ENSP00000506650.1:p.Thr161Ile
ENST00000680521.1:n.2132C>T
ENST00000680792.1:c.668C>T	ENSP00000506012.1:p.Thr223Ile
ENST00000680815.1:n.3628C>T
ENST00000680911.1:c.627-31C>T	ENSP00000506556.1:n.627-31C>T
ENST00000680990.1:c.*440C>T	ENSP00000506050.1:n.*440C>T
ENST00000681129.1:c.482C>T	ENSP00000505329.1:p.Thr161Ile
ENST00000681193.1:n.2910C>T
ENST00000681389.1:n.2000C>T
ENST00000681414.1:c.587C>T	ENSP00000505797.1:p.Thr196Ile
ENST00000681441.1:c.*212C>T	ENSP00000504992.1:n.*212C>T
ENST00000681539.1:c.668C>T	ENSP00000505557.1:p.Thr223Ile
ENST00000681551.1:c.668C>T	ENSP00000504974.1:p.Thr223Ile
ENST00000681636.1:c.668C>T	ENSP00000506155.1:p.Thr223Ile
ENST00000681742.1:c.668C>T	ENSP00000506122.1:p.Thr223Ile
ENST00000681777.1:c.*36C>T	ENSP00000506511.1:n.*36C>T
ENST00000354200.4:c.668C>T	ENSP00000346139.4:p.Thr223Ile
ENST00000461188.5:n.1545C>T
ENST00000461304.5:c.668C>T	ENSP00000432280.1:p.Thr223Ile
ENST00000494633.1:n.973C>T
NM_144628.3:c.668C>T	NP_653229.1:p.Thr223Ile
NR_111901.1:n.816C>T
XM_005260661.1:c.668C>T	XP_005260718.1:p.Thr223Ile
XM_006723540.2:c.482C>T	XP_006723603.1:p.Thr161Ile
XM_006723540.3:c.482C>T	XP_006723603.1:p.Thr161Ile
XM_017027645.1:c.482C>T	XP_016883134.1:p.Thr161Ile
NM_144628.4:c.668C>T MANE Select	NP_653229.1:p.Thr223Ile
NR_111901.2:n.796C>T