Canonical Allele Identifier: CA1932021481

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989675C= , CM000672.2:g.100989675C=	GRCh38
NC_000010.10:g.102749432C= , CM000672.1:g.102749432C=	GRCh37
NC_000010.9:g.102739422C=	NCBI36
NG_011646.1:g.2841G=
NG_012624.1:g.7140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1275C= MANE Select	ENSP00000309595.2:p.Ile425=
ENST00000370228.2:c.1275C=	ENSP00000359248.1:p.Ile425=
ENST00000643860.1:c.1275C=	ENSP00000494389.1:p.Ile425=
ENST00000646226.1:n.90C=
ENST00000647109.1:c.32C=
ENST00000650396.1:c.267-31C=
ENST00000311916.6:c.1275C=	ENSP00000309595.2:p.Ile425=
ENST00000370228.1:c.1275C=	ENSP00000359248.1:p.Ile425=
ENST00000459764.1:n.118C=
ENST00000473656.5:n.96C=
ENST00000476766.5:n.192-31C=
NM_001163812.1:c.1275C=	NP_001157284.1:p.Ile425=
NM_001163813.1:c.-88C=	NP_001157285.1:n.-88C=
NM_001163814.1:c.-88C=	NP_001157286.1:n.-88C=
NM_021830.4:c.1275C=	NP_068602.2:p.Ile425=
XM_011539974.1:c.-57-31C=	XP_011538276.1:n.-57-31C=
XM_011539975.1:c.-57-31C=	XP_011538277.1:n.-57-31C=
XR_945788.1:n.2077-31C=
XM_011539975.2:c.-57-31C=	XP_011538277.1:n.-57-31C=
XM_017016437.1:c.-57-31C=	XP_016871926.1:n.-57-31C=
XR_001747142.1:n.1449C=
XR_001747144.1:n.1418-31C=
XR_002956991.1:n.1418-31C=
XR_945788.2:n.1418-31C=
NM_021830.5:c.1275C= MANE Select	NP_068602.2:p.Ile425=
NM_001163812.2:c.1275C=	NP_001157284.1:p.Ile425=
NM_001163813.2:c.-88C=	NP_001157285.1:n.-88C=
NM_001163814.2:c.-88C=	NP_001157286.1:n.-88C=
NM_001368275.1:c.-57-31C=	NP_001355204.1:n.-57-31C=
NR_160738.1:n.1943C=
NR_160739.1:n.103C=
NR_160740.1:n.1912-31C=
NR_160741.1:n.1912-31C=
NR_160742.1:n.1912-31C=