Canonical Allele Identifier: CA378207325

Gene: TWNK

Linked Data

• ClinVar Variation Id: 2014193
• ClinVar RCV Id: RCV002861370
• COSMIC: COSM5660226
• MyVariant Identifiers: chr10:g.102748383G>T (hg19) ; chr10:g.100988626G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988626G>T , CM000672.2:g.100988626G>T	GRCh38
NC_000010.10:g.102748383G>T , CM000672.1:g.102748383G>T	GRCh37
NC_000010.9:g.102738373G>T	NCBI36
NG_011646.1:g.3890C>A
NG_012624.1:g.6091G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.416G>T MANE Select	ENSP00000309595.2:p.Gly139Val
ENST00000370228.2:c.416G>T	ENSP00000359248.1:p.Gly139Val
ENST00000643860.1:c.416G>T	ENSP00000494389.1:p.Gly139Val
ENST00000646226.1:n.58+1013G>T
ENST00000311916.6:c.416G>T	ENSP00000309595.2:p.Gly139Val
ENST00000370228.1:c.416G>T	ENSP00000359248.1:p.Gly139Val
ENST00000459764.1:n.86+746G>T
ENST00000473656.5:n.64+1013G>T
ENST00000476766.5:n.191+1069G>T
NM_001163812.1:c.416G>T	NP_001157284.1:p.Gly139Val
NM_001163813.1:c.-120+1013G>T	NP_001157285.1:n.-120+1013G>T
NM_001163814.1:c.-120+1013G>T	NP_001157286.1:n.-120+1013G>T
NM_021830.4:c.416G>T	NP_068602.2:p.Gly139Val
XM_011539975.1:c.-58+1013G>T	XP_011538277.1:n.-58+1013G>T
XR_945788.1:n.1249G>T
XM_011539975.2:c.-58+1013G>T	XP_011538277.1:n.-58+1013G>T
XM_017016437.1:c.-885G>T	XP_016871926.1:n.-885G>T
XR_001747142.1:n.590G>T
XR_001747144.1:n.590G>T
XR_002956991.1:n.590G>T
XR_945788.2:n.590G>T
NM_021830.5:c.416G>T MANE Select	NP_068602.2:p.Gly139Val
NM_001163812.2:c.416G>T	NP_001157284.1:p.Gly139Val
NM_001163813.2:c.-120+1013G>T	NP_001157285.1:n.-120+1013G>T
NM_001163814.2:c.-120+1013G>T	NP_001157286.1:n.-120+1013G>T
NM_001368275.1:c.-58+1013G>T	NP_001355204.1:n.-58+1013G>T
NR_160738.1:n.1084G>T
NR_160739.1:n.71+1013G>T
NR_160740.1:n.1084G>T
NR_160741.1:n.1084G>T
NR_160742.1:n.1084G>T