Canonical Allele Identifier: CA378210980

Gene: TWNK

Linked Data

• MyVariant Identifiers: chr10:g.102749626G>T (hg19) ; chr10:g.100989869G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989869G>T , CM000672.2:g.100989869G>T	GRCh38
NC_000010.10:g.102749626G>T , CM000672.1:g.102749626G>T	GRCh37
NC_000010.9:g.102739616G>T	NCBI36
NG_011646.1:g.2647C>A
NG_012624.1:g.7334G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1469G>T MANE Select	ENSP00000309595.2:p.Gly490Val
ENST00000370228.2:c.1469G>T	ENSP00000359248.1:p.Gly490Val
ENST00000643860.1:c.1469G>T	ENSP00000494389.1:p.Gly490Val
ENST00000646226.1:n.284G>T
ENST00000647109.1:c.128G>T
ENST00000650396.1:c.430G>T
ENST00000311916.6:c.1469G>T	ENSP00000309595.2:p.Gly490Val
ENST00000370228.1:c.1469G>T	ENSP00000359248.1:p.Gly490Val
ENST00000459764.1:n.312G>T
ENST00000473656.5:n.290G>T
ENST00000476766.5:n.355G>T
NM_001163812.1:c.1469G>T	NP_001157284.1:p.Gly490Val
NM_001163813.1:c.107G>T	NP_001157285.1:p.Gly36Val
NM_001163814.1:c.107G>T	NP_001157286.1:p.Gly36Val
NM_021830.4:c.1469G>T	NP_068602.2:p.Gly490Val
XM_011539974.1:c.107G>T	XP_011538276.1:p.Gly36Val
XM_011539975.1:c.107G>T	XP_011538277.1:p.Gly36Val
XR_945788.1:n.2240G>T
XM_011539975.2:c.107G>T	XP_011538277.1:p.Gly36Val
XM_017016437.1:c.107G>T	XP_016871926.1:p.Gly36Val
XR_001747142.1:n.1643G>T
XR_001747144.1:n.1581G>T
XR_002956991.1:n.1581G>T
XR_945788.2:n.1581G>T
NM_021830.5:c.1469G>T MANE Select	NP_068602.2:p.Gly490Val
NM_001163812.2:c.1469G>T	NP_001157284.1:p.Gly490Val
NM_001163813.2:c.107G>T	NP_001157285.1:p.Gly36Val
NM_001163814.2:c.107G>T	NP_001157286.1:p.Gly36Val
NM_001368275.1:c.107G>T	NP_001355204.1:p.Gly36Val
NR_160738.1:n.2137G>T
NR_160739.1:n.297G>T
NR_160740.1:n.2075G>T
NR_160741.1:n.2075G>T
NR_160742.1:n.2075G>T