Canonical Allele Identifier: CA1932021590

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989712A= , CM000672.2:g.100989712A=	GRCh38
NC_000010.10:g.102749469A= , CM000672.1:g.102749469A=	GRCh37
NC_000010.9:g.102739459A=	NCBI36
NG_011646.1:g.2804T=
NG_012624.1:g.7177A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1312A= MANE Select	ENSP00000309595.2:p.Asn438=
ENST00000370228.2:c.1312A=	ENSP00000359248.1:p.Asn438=
ENST00000643860.1:c.1312A=	ENSP00000494389.1:p.Asn438=
ENST00000646226.1:n.127A=
ENST00000647109.1:c.33+36A=
ENST00000650396.1:c.273A=
ENST00000311916.6:c.1312A=	ENSP00000309595.2:p.Asn438=
ENST00000370228.1:c.1312A=	ENSP00000359248.1:p.Asn438=
ENST00000459764.1:n.155A=
ENST00000473656.5:n.133A=
ENST00000476766.5:n.198A=
NM_001163812.1:c.1312A=	NP_001157284.1:p.Asn438=
NM_001163813.1:c.-51A=	NP_001157285.1:n.-51A=
NM_001163814.1:c.-51A=	NP_001157286.1:n.-51A=
NM_021830.4:c.1312A=	NP_068602.2:p.Asn438=
XM_011539974.1:c.-51A=	XP_011538276.1:n.-51A=
XM_011539975.1:c.-51A=	XP_011538277.1:n.-51A=
XR_945788.1:n.2083A=
XM_011539975.2:c.-51A=	XP_011538277.1:n.-51A=
XM_017016437.1:c.-51A=	XP_016871926.1:n.-51A=
XR_001747142.1:n.1486A=
XR_001747144.1:n.1424A=
XR_002956991.1:n.1424A=
XR_945788.2:n.1424A=
NM_021830.5:c.1312A= MANE Select	NP_068602.2:p.Asn438=
NM_001163812.2:c.1312A=	NP_001157284.1:p.Asn438=
NM_001163813.2:c.-51A=	NP_001157285.1:n.-51A=
NM_001163814.2:c.-51A=	NP_001157286.1:n.-51A=
NM_001368275.1:c.-51A=	NP_001355204.1:n.-51A=
NR_160738.1:n.1980A=
NR_160739.1:n.140A=
NR_160740.1:n.1918A=
NR_160741.1:n.1918A=
NR_160742.1:n.1918A=