Canonical Allele Identifier: CA1932021763

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989779C= , CM000672.2:g.100989779C=	GRCh38
NC_000010.10:g.102749536C= , CM000672.1:g.102749536C=	GRCh37
NC_000010.9:g.102739526C=	NCBI36
NG_011646.1:g.2737G=
NG_012624.1:g.7244C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1379C= MANE Select	ENSP00000309595.2:p.Ala460=
ENST00000370228.2:c.1379C=	ENSP00000359248.1:p.Ala460=
ENST00000643860.1:c.1379C=	ENSP00000494389.1:p.Ala460=
ENST00000646226.1:n.194C=
ENST00000647109.1:c.38C=
ENST00000650396.1:c.340C=
ENST00000311916.6:c.1379C=	ENSP00000309595.2:p.Ala460=
ENST00000370228.1:c.1379C=	ENSP00000359248.1:p.Ala460=
ENST00000459764.1:n.222C=
ENST00000473656.5:n.200C=
ENST00000476766.5:n.265C=
NM_001163812.1:c.1379C=	NP_001157284.1:p.Ala460=
NM_001163813.1:c.17C=	NP_001157285.1:p.Ala6=
NM_001163814.1:c.17C=	NP_001157286.1:p.Ala6=
NM_021830.4:c.1379C=	NP_068602.2:p.Ala460=
XM_011539974.1:c.17C=	XP_011538276.1:p.Ala6=
XM_011539975.1:c.17C=	XP_011538277.1:p.Ala6=
XR_945788.1:n.2150C=
XM_011539975.2:c.17C=	XP_011538277.1:p.Ala6=
XM_017016437.1:c.17C=	XP_016871926.1:p.Ala6=
XR_001747142.1:n.1553C=
XR_001747144.1:n.1491C=
XR_002956991.1:n.1491C=
XR_945788.2:n.1491C=
NM_021830.5:c.1379C= MANE Select	NP_068602.2:p.Ala460=
NM_001163812.2:c.1379C=	NP_001157284.1:p.Ala460=
NM_001163813.2:c.17C=	NP_001157285.1:p.Ala6=
NM_001163814.2:c.17C=	NP_001157286.1:p.Ala6=
NM_001368275.1:c.17C=	NP_001355204.1:p.Ala6=
NR_160738.1:n.2047C=
NR_160739.1:n.207C=
NR_160740.1:n.1985C=
NR_160741.1:n.1985C=
NR_160742.1:n.1985C=