Canonical Allele Identifier: CA1932018442

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988548G= , CM000672.2:g.100988548G=	GRCh38
NC_000010.10:g.102748305G= , CM000672.1:g.102748305G=	GRCh37
NC_000010.9:g.102738295G=	NCBI36
NG_011646.1:g.3968C=
NG_012624.1:g.6013G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.338G= MANE Select	ENSP00000309595.2:p.Cys113=
ENST00000370228.2:c.338G=	ENSP00000359248.1:p.Cys113=
ENST00000643860.1:c.338G=	ENSP00000494389.1:p.Cys113=
ENST00000646226.1:n.58+935G=
ENST00000311916.6:c.338G=	ENSP00000309595.2:p.Cys113=
ENST00000370228.1:c.338G=	ENSP00000359248.1:p.Cys113=
ENST00000459764.1:n.86+668G=
ENST00000473656.5:n.64+935G=
ENST00000476766.5:n.191+991G=
NM_001163812.1:c.338G=	NP_001157284.1:p.Cys113=
NM_001163813.1:c.-120+935G=	NP_001157285.1:n.-120+935G=
NM_001163814.1:c.-120+935G=	NP_001157286.1:n.-120+935G=
NM_021830.4:c.338G=	NP_068602.2:p.Cys113=
XM_011539975.1:c.-58+935G=	XP_011538277.1:n.-58+935G=
XR_945788.1:n.1171G=
XM_011539975.2:c.-58+935G=	XP_011538277.1:n.-58+935G=
XM_017016437.1:c.-963G=	XP_016871926.1:n.-963G=
XR_001747142.1:n.512G=
XR_001747144.1:n.512G=
XR_002956991.1:n.512G=
XR_945788.2:n.512G=
NM_021830.5:c.338G= MANE Select	NP_068602.2:p.Cys113=
NM_001163812.2:c.338G=	NP_001157284.1:p.Cys113=
NM_001163813.2:c.-120+935G=	NP_001157285.1:n.-120+935G=
NM_001163814.2:c.-120+935G=	NP_001157286.1:n.-120+935G=
NM_001368275.1:c.-58+935G=	NP_001355204.1:n.-58+935G=
NR_160738.1:n.1006G=
NR_160739.1:n.71+935G=
NR_160740.1:n.1006G=
NR_160741.1:n.1006G=
NR_160742.1:n.1006G=