Canonical Allele Identifier: CA116968

Gene: TWNK

Linked Data

• ClinVar Variation Id: 4625
• ClinVar RCV Id: RCV000004888 ; RCV000020867
• dbSNP Id: rs80356543
• MyVariant Identifiers: chr10:g.102748922A>G (hg19) ; chr10:g.100989165A>G (hg38)
• PubMed: PMID:15668446 ; PMID:20301746

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989165A>G , CM000672.2:g.100989165A>G	GRCh38
NC_000010.10:g.102748922A>G , CM000672.1:g.102748922A>G	GRCh37
NC_000010.9:g.102738912A>G	NCBI36
NG_011646.1:g.3351T>C
NG_012624.1:g.6630A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.955A>G MANE Select	ENSP00000309595.2:p.Lys319Glu
ENST00000370228.2:c.955A>G	ENSP00000359248.1:p.Lys319Glu
ENST00000643860.1:c.955A>G	ENSP00000494389.1:p.Lys319Glu
ENST00000646226.1:n.59-479A>G
ENST00000311916.6:c.955A>G	ENSP00000309595.2:p.Lys319Glu
ENST00000370228.1:c.955A>G	ENSP00000359248.1:p.Lys319Glu
ENST00000459764.1:n.87-479A>G
ENST00000473656.5:n.65-479A>G
ENST00000476766.5:n.192-541A>G
NM_001163812.1:c.955A>G	NP_001157284.1:p.Lys319Glu
NM_001163813.1:c.-119-479A>G	NP_001157285.1:n.-119-479A>G
NM_001163814.1:c.-119-479A>G	NP_001157286.1:n.-119-479A>G
NM_021830.4:c.955A>G	NP_068602.2:p.Lys319Glu
XM_011539975.1:c.-57-541A>G	XP_011538277.1:n.-57-541A>G
XR_945788.1:n.1788A>G
XM_011539975.2:c.-57-541A>G	XP_011538277.1:n.-57-541A>G
XM_017016437.1:c.-346A>G	XP_016871926.1:n.-346A>G
XR_001747142.1:n.1129A>G
XR_001747144.1:n.1129A>G
XR_002956991.1:n.1129A>G
XR_945788.2:n.1129A>G
NM_021830.5:c.955A>G MANE Select	NP_068602.2:p.Lys319Glu
NM_001163812.2:c.955A>G	NP_001157284.1:p.Lys319Glu
NM_001163813.2:c.-119-479A>G	NP_001157285.1:n.-119-479A>G
NM_001163814.2:c.-119-479A>G	NP_001157286.1:n.-119-479A>G
NM_001368275.1:c.-57-541A>G	NP_001355204.1:n.-57-541A>G
NR_160738.1:n.1623A>G
NR_160739.1:n.72-479A>G
NR_160740.1:n.1623A>G
NR_160741.1:n.1623A>G
NR_160742.1:n.1623A>G