Canonical Allele Identifier: CA2610574243

Gene: TWNK

Linked Data

• gnomAD v4: 10-100990659-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100990659T>G , CM000672.2:g.100990659T>G	GRCh38
NC_000010.10:g.102750416T>G , CM000672.1:g.102750416T>G	GRCh37
NC_000010.9:g.102740406T>G	NCBI36
NG_011646.1:g.1857A>C
NG_012624.1:g.8124T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1592+116T>G MANE Select	ENSP00000309595.2:n.1592+116T>G
ENST00000370228.2:c.1592+116T>G	ENSP00000359248.1:n.1592+116T>G
ENST00000643860.1:c.*112T>G	ENSP00000494389.1:n.*112T>G
ENST00000646226.1:n.407+116T>G
ENST00000647109.1:c.251+116T>G
ENST00000650396.1:c.669T>G
ENST00000311916.6:c.1592+116T>G	ENSP00000309595.2:n.1592+116T>G
ENST00000370228.1:c.1592+116T>G	ENSP00000359248.1:n.1592+116T>G
ENST00000473656.5:n.413+116T>G
ENST00000476766.5:n.478+116T>G
NM_001163812.1:c.1592+116T>G	NP_001157284.1:n.1592+116T>G
NM_001163813.1:c.230+116T>G	NP_001157285.1:n.230+116T>G
NM_001163814.1:c.230+116T>G	NP_001157286.1:n.230+116T>G
NM_021830.4:c.1592+116T>G	NP_068602.2:n.1592+116T>G
XM_011539974.1:c.230+116T>G	XP_011538276.1:n.230+116T>G
XM_011539975.1:c.230+116T>G	XP_011538277.1:n.230+116T>G
XR_945788.1:n.2363+116T>G
XM_011539975.2:c.230+116T>G	XP_011538277.1:n.230+116T>G
XM_017016437.1:c.230+116T>G	XP_016871926.1:n.230+116T>G
XR_001747142.1:n.1882T>G
XR_001747144.1:n.1820T>G
XR_002956991.1:n.1704+116T>G
XR_945788.2:n.1704+116T>G
NM_021830.5:c.1592+116T>G MANE Select	NP_068602.2:n.1592+116T>G
NM_001163812.2:c.1592+116T>G	NP_001157284.1:n.1592+116T>G
NM_001163813.2:c.230+116T>G	NP_001157285.1:n.230+116T>G
NM_001163814.2:c.230+116T>G	NP_001157286.1:n.230+116T>G
NM_001368275.1:c.230+116T>G	NP_001355204.1:n.230+116T>G
NR_160738.1:n.2376T>G
NR_160739.1:n.536T>G
NR_160740.1:n.2198+116T>G
NR_160741.1:n.2198+116T>G
NR_160742.1:n.2314T>G