Canonical Allele Identifier: CA378210899

Gene: TWNK

Linked Data

• dbSNP Id: rs1085307937
• COSMIC: COSM1296857
• MyVariant Identifiers: chr10:g.102749592G>C (hg19) ; chr10:g.100989835G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989835G>C , CM000672.2:g.100989835G>C	GRCh38
NC_000010.10:g.102749592G>C , CM000672.1:g.102749592G>C	GRCh37
NC_000010.9:g.102739582G>C	NCBI36
NG_011646.1:g.2681C>G
NG_012624.1:g.7300G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1435G>C MANE Select	ENSP00000309595.2:p.Glu479Gln
ENST00000370228.2:c.1435G>C	ENSP00000359248.1:p.Glu479Gln
ENST00000643860.1:c.1435G>C	ENSP00000494389.1:p.Glu479Gln
ENST00000646226.1:n.250G>C
ENST00000647109.1:c.94G>C
ENST00000650396.1:c.396G>C
ENST00000311916.6:c.1435G>C	ENSP00000309595.2:p.Glu479Gln
ENST00000370228.1:c.1435G>C	ENSP00000359248.1:p.Glu479Gln
ENST00000459764.1:n.278G>C
ENST00000473656.5:n.256G>C
ENST00000476766.5:n.321G>C
NM_001163812.1:c.1435G>C	NP_001157284.1:p.Glu479Gln
NM_001163813.1:c.73G>C	NP_001157285.1:p.Glu25Gln
NM_001163814.1:c.73G>C	NP_001157286.1:p.Glu25Gln
NM_021830.4:c.1435G>C	NP_068602.2:p.Glu479Gln
XM_011539974.1:c.73G>C	XP_011538276.1:p.Glu25Gln
XM_011539975.1:c.73G>C	XP_011538277.1:p.Glu25Gln
XR_945788.1:n.2206G>C
XM_011539975.2:c.73G>C	XP_011538277.1:p.Glu25Gln
XM_017016437.1:c.73G>C	XP_016871926.1:p.Glu25Gln
XR_001747142.1:n.1609G>C
XR_001747144.1:n.1547G>C
XR_002956991.1:n.1547G>C
XR_945788.2:n.1547G>C
NM_021830.5:c.1435G>C MANE Select	NP_068602.2:p.Glu479Gln
NM_001163812.2:c.1435G>C	NP_001157284.1:p.Glu479Gln
NM_001163813.2:c.73G>C	NP_001157285.1:p.Glu25Gln
NM_001163814.2:c.73G>C	NP_001157286.1:p.Glu25Gln
NM_001368275.1:c.73G>C	NP_001355204.1:p.Glu25Gln
NR_160738.1:n.2103G>C
NR_160739.1:n.263G>C
NR_160740.1:n.2041G>C
NR_160741.1:n.2041G>C
NR_160742.1:n.2041G>C