Canonical Allele Identifier: CA407944677

Gene: TBC1D20

Linked Data

• MyVariant Identifiers: chr20:g.420995A>T (hg19) ; chr20:g.440351A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.440351A>T , CM000682.2:g.440351A>T	GRCh38
NC_000020.10:g.420995A>T , CM000682.1:g.420995A>T	GRCh37
NC_000020.9:g.368995A>T	NCBI36
NG_034082.1:g.27203T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354200.5:c.665T>A MANE Select	ENSP00000346139.4:p.Ile222Asn
ENST00000461188.6:n.1905T>A
ENST00000679451.1:n.893-34T>A
ENST00000679741.1:c.665T>A	ENSP00000504904.1:p.Ile222Asn
ENST00000679895.1:c.761T>A	ENSP00000505197.1:p.Ile254Asn
ENST00000679944.1:c.665T>A	ENSP00000506278.1:p.Ile222Asn
ENST00000679953.1:n.1554T>A
ENST00000679973.1:c.627-34T>A	ENSP00000506502.1:n.627-34T>A
ENST00000680050.1:c.479T>A	ENSP00000505464.1:p.Ile160Asn
ENST00000680088.1:n.810T>A
ENST00000680106.1:c.665T>A	ENSP00000505500.1:p.Ile222Asn
ENST00000680284.1:c.665T>A	ENSP00000506231.1:p.Ile222Asn
ENST00000680491.1:n.2156T>A
ENST00000680515.1:c.479T>A	ENSP00000506650.1:p.Ile160Asn
ENST00000680521.1:n.2129T>A
ENST00000680792.1:c.665T>A	ENSP00000506012.1:p.Ile222Asn
ENST00000680815.1:n.3625T>A
ENST00000680911.1:c.627-34T>A	ENSP00000506556.1:n.627-34T>A
ENST00000680990.1:c.*437T>A	ENSP00000506050.1:n.*437T>A
ENST00000681129.1:c.479T>A	ENSP00000505329.1:p.Ile160Asn
ENST00000681193.1:n.2907T>A
ENST00000681389.1:n.1997T>A
ENST00000681414.1:c.584T>A	ENSP00000505797.1:p.Ile195Asn
ENST00000681441.1:c.*209T>A	ENSP00000504992.1:n.*209T>A
ENST00000681539.1:c.665T>A	ENSP00000505557.1:p.Ile222Asn
ENST00000681551.1:c.665T>A	ENSP00000504974.1:p.Ile222Asn
ENST00000681636.1:c.665T>A	ENSP00000506155.1:p.Ile222Asn
ENST00000681742.1:c.665T>A	ENSP00000506122.1:p.Ile222Asn
ENST00000681777.1:c.*33T>A	ENSP00000506511.1:n.*33T>A
ENST00000354200.4:c.665T>A	ENSP00000346139.4:p.Ile222Asn
ENST00000461188.5:n.1542T>A
ENST00000461304.5:c.665T>A	ENSP00000432280.1:p.Ile222Asn
ENST00000494633.1:n.970T>A
NM_144628.3:c.665T>A	NP_653229.1:p.Ile222Asn
NR_111901.1:n.813T>A
XM_005260661.1:c.665T>A	XP_005260718.1:p.Ile222Asn
XM_006723540.2:c.479T>A	XP_006723603.1:p.Ile160Asn
XM_006723540.3:c.479T>A	XP_006723603.1:p.Ile160Asn
XM_017027645.1:c.479T>A	XP_016883134.1:p.Ile160Asn
NM_144628.4:c.665T>A MANE Select	NP_653229.1:p.Ile222Asn
NR_111901.2:n.793T>A