Canonical Allele Identifier: CA1932018318

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988490A= , CM000672.2:g.100988490A=	GRCh38
NC_000010.10:g.102748247A= , CM000672.1:g.102748247A=	GRCh37
NC_000010.9:g.102738237A=	NCBI36
NG_011646.1:g.4026T=
NG_012624.1:g.5955A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.280A= MANE Select	ENSP00000309595.2:p.Thr94=
ENST00000370228.2:c.280A=	ENSP00000359248.1:p.Thr94=
ENST00000643860.1:c.280A=	ENSP00000494389.1:p.Thr94=
ENST00000646226.1:n.58+877A=
ENST00000311916.6:c.280A=	ENSP00000309595.2:p.Thr94=
ENST00000370228.1:c.280A=	ENSP00000359248.1:p.Thr94=
ENST00000459764.1:n.86+610A=
ENST00000473656.5:n.64+877A=
ENST00000476766.5:n.191+933A=
NM_001163812.1:c.280A=	NP_001157284.1:p.Thr94=
NM_001163813.1:c.-120+877A=	NP_001157285.1:n.-120+877A=
NM_001163814.1:c.-120+877A=	NP_001157286.1:n.-120+877A=
NM_021830.4:c.280A=	NP_068602.2:p.Thr94=
XM_011539975.1:c.-58+877A=	XP_011538277.1:n.-58+877A=
XR_945788.1:n.1113A=
XM_011539975.2:c.-58+877A=	XP_011538277.1:n.-58+877A=
XM_017016437.1:c.-1021A=	XP_016871926.1:n.-1021A=
XR_001747142.1:n.454A=
XR_001747144.1:n.454A=
XR_002956991.1:n.454A=
XR_945788.2:n.454A=
NM_021830.5:c.280A= MANE Select	NP_068602.2:p.Thr94=
NM_001163812.2:c.280A=	NP_001157284.1:p.Thr94=
NM_001163813.2:c.-120+877A=	NP_001157285.1:n.-120+877A=
NM_001163814.2:c.-120+877A=	NP_001157286.1:n.-120+877A=
NM_001368275.1:c.-58+877A=	NP_001355204.1:n.-58+877A=
NR_160738.1:n.948A=
NR_160739.1:n.71+877A=
NR_160740.1:n.948A=
NR_160741.1:n.948A=
NR_160742.1:n.948A=