Canonical Allele Identifier: CA1932018353

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988495T= , CM000672.2:g.100988495T=	GRCh38
NC_000010.10:g.102748252T= , CM000672.1:g.102748252T=	GRCh37
NC_000010.9:g.102738242T=	NCBI36
NG_011646.1:g.4021A=
NG_012624.1:g.5960T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.285T= MANE Select	ENSP00000309595.2:p.Gly95=
ENST00000370228.2:c.285T=	ENSP00000359248.1:p.Gly95=
ENST00000643860.1:c.285T=	ENSP00000494389.1:p.Gly95=
ENST00000646226.1:n.58+882T=
ENST00000311916.6:c.285T=	ENSP00000309595.2:p.Gly95=
ENST00000370228.1:c.285T=	ENSP00000359248.1:p.Gly95=
ENST00000459764.1:n.86+615T=
ENST00000473656.5:n.64+882T=
ENST00000476766.5:n.191+938T=
NM_001163812.1:c.285T=	NP_001157284.1:p.Gly95=
NM_001163813.1:c.-120+882T=	NP_001157285.1:n.-120+882T=
NM_001163814.1:c.-120+882T=	NP_001157286.1:n.-120+882T=
NM_021830.4:c.285T=	NP_068602.2:p.Gly95=
XM_011539975.1:c.-58+882T=	XP_011538277.1:n.-58+882T=
XR_945788.1:n.1118T=
XM_011539975.2:c.-58+882T=	XP_011538277.1:n.-58+882T=
XM_017016437.1:c.-1016T=	XP_016871926.1:n.-1016T=
XR_001747142.1:n.459T=
XR_001747144.1:n.459T=
XR_002956991.1:n.459T=
XR_945788.2:n.459T=
NM_021830.5:c.285T= MANE Select	NP_068602.2:p.Gly95=
NM_001163812.2:c.285T=	NP_001157284.1:p.Gly95=
NM_001163813.2:c.-120+882T=	NP_001157285.1:n.-120+882T=
NM_001163814.2:c.-120+882T=	NP_001157286.1:n.-120+882T=
NM_001368275.1:c.-58+882T=	NP_001355204.1:n.-58+882T=
NR_160738.1:n.953T=
NR_160739.1:n.71+882T=
NR_160740.1:n.953T=
NR_160741.1:n.953T=
NR_160742.1:n.953T=