Canonical Allele Identifier: CA1932018378

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988515T= , CM000672.2:g.100988515T=	GRCh38
NC_000010.10:g.102748272T= , CM000672.1:g.102748272T=	GRCh37
NC_000010.9:g.102738262T=	NCBI36
NG_011646.1:g.4001A=
NG_012624.1:g.5980T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.305T= MANE Select	ENSP00000309595.2:p.Leu102=
ENST00000370228.2:c.305T=	ENSP00000359248.1:p.Leu102=
ENST00000643860.1:c.305T=	ENSP00000494389.1:p.Leu102=
ENST00000646226.1:n.58+902T=
ENST00000311916.6:c.305T=	ENSP00000309595.2:p.Leu102=
ENST00000370228.1:c.305T=	ENSP00000359248.1:p.Leu102=
ENST00000459764.1:n.86+635T=
ENST00000473656.5:n.64+902T=
ENST00000476766.5:n.191+958T=
NM_001163812.1:c.305T=	NP_001157284.1:p.Leu102=
NM_001163813.1:c.-120+902T=	NP_001157285.1:n.-120+902T=
NM_001163814.1:c.-120+902T=	NP_001157286.1:n.-120+902T=
NM_021830.4:c.305T=	NP_068602.2:p.Leu102=
XM_011539975.1:c.-58+902T=	XP_011538277.1:n.-58+902T=
XR_945788.1:n.1138T=
XM_011539975.2:c.-58+902T=	XP_011538277.1:n.-58+902T=
XM_017016437.1:c.-996T=	XP_016871926.1:n.-996T=
XR_001747142.1:n.479T=
XR_001747144.1:n.479T=
XR_002956991.1:n.479T=
XR_945788.2:n.479T=
NM_021830.5:c.305T= MANE Select	NP_068602.2:p.Leu102=
NM_001163812.2:c.305T=	NP_001157284.1:p.Leu102=
NM_001163813.2:c.-120+902T=	NP_001157285.1:n.-120+902T=
NM_001163814.2:c.-120+902T=	NP_001157286.1:n.-120+902T=
NM_001368275.1:c.-58+902T=	NP_001355204.1:n.-58+902T=
NR_160738.1:n.973T=
NR_160739.1:n.71+902T=
NR_160740.1:n.973T=
NR_160741.1:n.973T=
NR_160742.1:n.973T=