Canonical Allele Identifier: CA212963388

Gene: TWNK

Linked Data

• dbSNP Id: rs772274141
• gnomAD v4: 10-100989563-C-G
• MyVariant Identifiers: chr10:g.102749320C>G (hg19) ; chr10:g.100989563C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989563C>G , CM000672.2:g.100989563C>G	GRCh38
NC_000010.10:g.102749320C>G , CM000672.1:g.102749320C>G	GRCh37
NC_000010.9:g.102739310C>G	NCBI36
NG_011646.1:g.2953G>C
NG_012624.1:g.7028C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1244-81C>G MANE Select	ENSP00000309595.2:n.1244-81C>G
ENST00000370228.2:c.1244-81C>G	ENSP00000359248.1:n.1244-81C>G
ENST00000643860.1:c.1244-81C>G	ENSP00000494389.1:n.1244-81C>G
ENST00000646226.1:n.59-81C>G
ENST00000650396.1:c.266+110C>G
ENST00000311916.6:c.1244-81C>G	ENSP00000309595.2:n.1244-81C>G
ENST00000370228.1:c.1244-81C>G	ENSP00000359248.1:n.1244-81C>G
ENST00000459764.1:n.87-81C>G
ENST00000473656.5:n.65-81C>G
ENST00000476766.5:n.192-143C>G
NM_001163812.1:c.1244-81C>G	NP_001157284.1:n.1244-81C>G
NM_001163813.1:c.-119-81C>G	NP_001157285.1:n.-119-81C>G
NM_001163814.1:c.-119-81C>G	NP_001157286.1:n.-119-81C>G
NM_021830.4:c.1244-81C>G	NP_068602.2:n.1244-81C>G
XM_011539974.1:c.-58+110C>G	XP_011538276.1:n.-58+110C>G
XM_011539975.1:c.-57-143C>G	XP_011538277.1:n.-57-143C>G
XR_945788.1:n.2076+110C>G
XM_011539975.2:c.-57-143C>G	XP_011538277.1:n.-57-143C>G
XM_017016437.1:c.-58+110C>G	XP_016871926.1:n.-58+110C>G
XR_001747142.1:n.1418-81C>G
XR_001747144.1:n.1417+110C>G
XR_002956991.1:n.1417+110C>G
XR_945788.2:n.1417+110C>G
NM_021830.5:c.1244-81C>G MANE Select	NP_068602.2:n.1244-81C>G
NM_001163812.2:c.1244-81C>G	NP_001157284.1:n.1244-81C>G
NM_001163813.2:c.-119-81C>G	NP_001157285.1:n.-119-81C>G
NM_001163814.2:c.-119-81C>G	NP_001157286.1:n.-119-81C>G
NM_001368275.1:c.-57-143C>G	NP_001355204.1:n.-57-143C>G
NR_160738.1:n.1912-81C>G
NR_160739.1:n.72-81C>G
NR_160740.1:n.1911+110C>G
NR_160741.1:n.1911+110C>G
NR_160742.1:n.1911+110C>G