Canonical Allele Identifier: CA1932018769

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988675G= , CM000672.2:g.100988675G=	GRCh38
NC_000010.10:g.102748432G= , CM000672.1:g.102748432G=	GRCh37
NC_000010.9:g.102738422G=	NCBI36
NG_011646.1:g.3841C=
NG_012624.1:g.6140G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.465G= MANE Select	ENSP00000309595.2:p.Arg155=
ENST00000370228.2:c.465G=	ENSP00000359248.1:p.Arg155=
ENST00000643860.1:c.465G=	ENSP00000494389.1:p.Arg155=
ENST00000646226.1:n.59-969G=
ENST00000311916.6:c.465G=	ENSP00000309595.2:p.Arg155=
ENST00000370228.1:c.465G=	ENSP00000359248.1:p.Arg155=
ENST00000459764.1:n.86+795G=
ENST00000473656.5:n.65-969G=
ENST00000476766.5:n.192-1031G=
NM_001163812.1:c.465G=	NP_001157284.1:p.Arg155=
NM_001163813.1:c.-119-969G=	NP_001157285.1:n.-119-969G=
NM_001163814.1:c.-119-969G=	NP_001157286.1:n.-119-969G=
NM_021830.4:c.465G=	NP_068602.2:p.Arg155=
XM_011539975.1:c.-57-1031G=	XP_011538277.1:n.-57-1031G=
XR_945788.1:n.1298G=
XM_011539975.2:c.-57-1031G=	XP_011538277.1:n.-57-1031G=
XM_017016437.1:c.-836G=	XP_016871926.1:n.-836G=
XR_001747142.1:n.639G=
XR_001747144.1:n.639G=
XR_002956991.1:n.639G=
XR_945788.2:n.639G=
NM_021830.5:c.465G= MANE Select	NP_068602.2:p.Arg155=
NM_001163812.2:c.465G=	NP_001157284.1:p.Arg155=
NM_001163813.2:c.-119-969G=	NP_001157285.1:n.-119-969G=
NM_001163814.2:c.-119-969G=	NP_001157286.1:n.-119-969G=
NM_001368275.1:c.-57-1031G=	NP_001355204.1:n.-57-1031G=
NR_160738.1:n.1133G=
NR_160739.1:n.72-969G=
NR_160740.1:n.1133G=
NR_160741.1:n.1133G=
NR_160742.1:n.1133G=