Canonical Allele Identifier: CA14851195

Gene: TBC1D20

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.445413C>T , CM000682.2:g.445413C>T	GRCh38
NC_000020.10:g.426057C>T , CM000682.1:g.426057C>T	GRCh37
NC_000020.9:g.374057C>T	NCBI36
NG_034082.1:g.22141G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354200.5:c.257-283G>A MANE Select	ENSP00000346139.4:n.257-283G>A
ENST00000461188.6:n.212+2476G>A
ENST00000679451.1:n.356-283G>A
ENST00000679741.1:c.257-283G>A	ENSP00000504904.1:n.257-283G>A
ENST00000679895.1:c.257-283G>A	ENSP00000505197.1:n.257-283G>A
ENST00000679944.1:c.257-283G>A	ENSP00000506278.1:n.257-283G>A
ENST00000679953.1:n.356-283G>A
ENST00000679973.1:c.257-283G>A	ENSP00000506502.1:n.257-283G>A
ENST00000680050.1:c.71-283G>A	ENSP00000505464.1:n.71-283G>A
ENST00000680088.1:n.402-283G>A
ENST00000680106.1:c.257-283G>A	ENSP00000505500.1:n.257-283G>A
ENST00000680284.1:c.257-283G>A	ENSP00000506231.1:n.257-283G>A
ENST00000680491.1:n.383-283G>A
ENST00000680515.1:c.71-283G>A	ENSP00000506650.1:n.71-283G>A
ENST00000680521.1:n.356-283G>A
ENST00000680792.1:c.257-283G>A	ENSP00000506012.1:n.257-283G>A
ENST00000680911.1:c.257-283G>A	ENSP00000506556.1:n.257-283G>A
ENST00000680990.1:c.257-283G>A	ENSP00000506050.1:n.257-283G>A
ENST00000681129.1:c.71-283G>A	ENSP00000505329.1:n.71-283G>A
ENST00000681389.1:n.391-283G>A
ENST00000681414.1:c.256+2476G>A	ENSP00000505797.1:n.256+2476G>A
ENST00000681441.1:c.257-283G>A	ENSP00000504992.1:n.257-283G>A
ENST00000681539.1:c.257-283G>A	ENSP00000505557.1:n.257-283G>A
ENST00000681551.1:c.257-283G>A	ENSP00000504974.1:n.257-283G>A
ENST00000681636.1:c.257-283G>A	ENSP00000506155.1:n.257-283G>A
ENST00000681742.1:c.257-283G>A	ENSP00000506122.1:n.257-283G>A
ENST00000681777.1:c.257-283G>A	ENSP00000506511.1:n.257-283G>A
ENST00000354200.4:c.257-283G>A	ENSP00000346139.4:n.257-283G>A
ENST00000461304.5:c.257-283G>A	ENSP00000432280.1:n.257-283G>A
ENST00000494633.1:n.395-283G>A
NM_144628.3:c.257-283G>A	NP_653229.1:n.257-283G>A
NR_111901.1:n.405-283G>A
XM_005260661.1:c.257-283G>A	XP_005260718.1:n.257-283G>A
XM_006723540.2:c.71-283G>A	XP_006723603.1:n.71-283G>A
XM_006723540.3:c.71-283G>A	XP_006723603.1:n.71-283G>A
XM_017027645.1:c.71-283G>A	XP_016883134.1:n.71-283G>A
NM_144628.4:c.257-283G>A MANE Select	NP_653229.1:n.257-283G>A
NR_111901.2:n.385-283G>A