Canonical Allele Identifier: CA378210871

Gene: TWNK

Linked Data

• MyVariant Identifiers: chr10:g.102749578G>T (hg19) ; chr10:g.100989821G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989821G>T , CM000672.2:g.100989821G>T	GRCh38
NC_000010.10:g.102749578G>T , CM000672.1:g.102749578G>T	GRCh37
NC_000010.9:g.102739568G>T	NCBI36
NG_011646.1:g.2695C>A
NG_012624.1:g.7286G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1421G>T MANE Select	ENSP00000309595.2:p.Trp474Leu
ENST00000370228.2:c.1421G>T	ENSP00000359248.1:p.Trp474Leu
ENST00000643860.1:c.1421G>T	ENSP00000494389.1:p.Trp474Leu
ENST00000646226.1:n.236G>T
ENST00000647109.1:c.80G>T
ENST00000650396.1:c.382G>T
ENST00000311916.6:c.1421G>T	ENSP00000309595.2:p.Trp474Leu
ENST00000370228.1:c.1421G>T	ENSP00000359248.1:p.Trp474Leu
ENST00000459764.1:n.264G>T
ENST00000473656.5:n.242G>T
ENST00000476766.5:n.307G>T
NM_001163812.1:c.1421G>T	NP_001157284.1:p.Trp474Leu
NM_001163813.1:c.59G>T	NP_001157285.1:p.Trp20Leu
NM_001163814.1:c.59G>T	NP_001157286.1:p.Trp20Leu
NM_021830.4:c.1421G>T	NP_068602.2:p.Trp474Leu
XM_011539974.1:c.59G>T	XP_011538276.1:p.Trp20Leu
XM_011539975.1:c.59G>T	XP_011538277.1:p.Trp20Leu
XR_945788.1:n.2192G>T
XM_011539975.2:c.59G>T	XP_011538277.1:p.Trp20Leu
XM_017016437.1:c.59G>T	XP_016871926.1:p.Trp20Leu
XR_001747142.1:n.1595G>T
XR_001747144.1:n.1533G>T
XR_002956991.1:n.1533G>T
XR_945788.2:n.1533G>T
NM_021830.5:c.1421G>T MANE Select	NP_068602.2:p.Trp474Leu
NM_001163812.2:c.1421G>T	NP_001157284.1:p.Trp474Leu
NM_001163813.2:c.59G>T	NP_001157285.1:p.Trp20Leu
NM_001163814.2:c.59G>T	NP_001157286.1:p.Trp20Leu
NM_001368275.1:c.59G>T	NP_001355204.1:p.Trp20Leu
NR_160738.1:n.2089G>T
NR_160739.1:n.249G>T
NR_160740.1:n.2027G>T
NR_160741.1:n.2027G>T
NR_160742.1:n.2027G>T