Canonical Allele Identifier: CA1932021836

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989809A= , CM000672.2:g.100989809A=	GRCh38
NC_000010.10:g.102749566A= , CM000672.1:g.102749566A=	GRCh37
NC_000010.9:g.102739556A=	NCBI36
NG_011646.1:g.2707T=
NG_012624.1:g.7274A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1409A= MANE Select	ENSP00000309595.2:p.Lys470=
ENST00000370228.2:c.1409A=	ENSP00000359248.1:p.Lys470=
ENST00000643860.1:c.1409A=	ENSP00000494389.1:p.Lys470=
ENST00000646226.1:n.224A=
ENST00000647109.1:c.68A=
ENST00000650396.1:c.370A=
ENST00000311916.6:c.1409A=	ENSP00000309595.2:p.Lys470=
ENST00000370228.1:c.1409A=	ENSP00000359248.1:p.Lys470=
ENST00000459764.1:n.252A=
ENST00000473656.5:n.230A=
ENST00000476766.5:n.295A=
NM_001163812.1:c.1409A=	NP_001157284.1:p.Lys470=
NM_001163813.1:c.47A=	NP_001157285.1:p.Lys16=
NM_001163814.1:c.47A=	NP_001157286.1:p.Lys16=
NM_021830.4:c.1409A=	NP_068602.2:p.Lys470=
XM_011539974.1:c.47A=	XP_011538276.1:p.Lys16=
XM_011539975.1:c.47A=	XP_011538277.1:p.Lys16=
XR_945788.1:n.2180A=
XM_011539975.2:c.47A=	XP_011538277.1:p.Lys16=
XM_017016437.1:c.47A=	XP_016871926.1:p.Lys16=
XR_001747142.1:n.1583A=
XR_001747144.1:n.1521A=
XR_002956991.1:n.1521A=
XR_945788.2:n.1521A=
NM_021830.5:c.1409A= MANE Select	NP_068602.2:p.Lys470=
NM_001163812.2:c.1409A=	NP_001157284.1:p.Lys470=
NM_001163813.2:c.47A=	NP_001157285.1:p.Lys16=
NM_001163814.2:c.47A=	NP_001157286.1:p.Lys16=
NM_001368275.1:c.47A=	NP_001355204.1:p.Lys16=
NR_160738.1:n.2077A=
NR_160739.1:n.237A=
NR_160740.1:n.2015A=
NR_160741.1:n.2015A=
NR_160742.1:n.2015A=