Canonical Allele Identifier: CA1932021824

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989801A= , CM000672.2:g.100989801A=	GRCh38
NC_000010.10:g.102749558A= , CM000672.1:g.102749558A=	GRCh37
NC_000010.9:g.102739548A=	NCBI36
NG_011646.1:g.2715T=
NG_012624.1:g.7266A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1401A= MANE Select	ENSP00000309595.2:p.Gln467=
ENST00000370228.2:c.1401A=	ENSP00000359248.1:p.Gln467=
ENST00000643860.1:c.1401A=	ENSP00000494389.1:p.Gln467=
ENST00000646226.1:n.216A=
ENST00000647109.1:c.60A=
ENST00000650396.1:c.362A=
ENST00000311916.6:c.1401A=	ENSP00000309595.2:p.Gln467=
ENST00000370228.1:c.1401A=	ENSP00000359248.1:p.Gln467=
ENST00000459764.1:n.244A=
ENST00000473656.5:n.222A=
ENST00000476766.5:n.287A=
NM_001163812.1:c.1401A=	NP_001157284.1:p.Gln467=
NM_001163813.1:c.39A=	NP_001157285.1:p.Gln13=
NM_001163814.1:c.39A=	NP_001157286.1:p.Gln13=
NM_021830.4:c.1401A=	NP_068602.2:p.Gln467=
XM_011539974.1:c.39A=	XP_011538276.1:p.Gln13=
XM_011539975.1:c.39A=	XP_011538277.1:p.Gln13=
XR_945788.1:n.2172A=
XM_011539975.2:c.39A=	XP_011538277.1:p.Gln13=
XM_017016437.1:c.39A=	XP_016871926.1:p.Gln13=
XR_001747142.1:n.1575A=
XR_001747144.1:n.1513A=
XR_002956991.1:n.1513A=
XR_945788.2:n.1513A=
NM_021830.5:c.1401A= MANE Select	NP_068602.2:p.Gln467=
NM_001163812.2:c.1401A=	NP_001157284.1:p.Gln467=
NM_001163813.2:c.39A=	NP_001157285.1:p.Gln13=
NM_001163814.2:c.39A=	NP_001157286.1:p.Gln13=
NM_001368275.1:c.39A=	NP_001355204.1:p.Gln13=
NR_160738.1:n.2069A=
NR_160739.1:n.229A=
NR_160740.1:n.2007A=
NR_160741.1:n.2007A=
NR_160742.1:n.2007A=