Canonical Allele Identifier: CA1932021876

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989823G= , CM000672.2:g.100989823G=	GRCh38
NC_000010.10:g.102749580G= , CM000672.1:g.102749580G=	GRCh37
NC_000010.9:g.102739570G=	NCBI36
NG_011646.1:g.2693C=
NG_012624.1:g.7288G=

Transcript Alleles

HGVS	Amino-acid Change
NM_021830.5:c.1423G= MANE Select	NP_068602.2:p.Ala475=
ENST00000311916.8:c.1423G= MANE Select	ENSP00000309595.2:p.Ala475=
NM_001163812.1:c.1423G=	NP_001157284.1:p.Ala475=
NM_001163812.2:c.1423G=	NP_001157284.1:p.Ala475=
NM_001163813.1:c.61G=	NP_001157285.1:p.Ala21=
NM_001163813.2:c.61G=	NP_001157285.1:p.Ala21=
NM_001163814.1:c.61G=	NP_001157286.1:p.Ala21=
NM_001163814.2:c.61G=	NP_001157286.1:p.Ala21=
NM_001368275.1:c.61G=	NP_001355204.1:p.Ala21=
NM_021830.4:c.1423G=	NP_068602.2:p.Ala475=
NR_160738.1:n.2091G=
NR_160739.1:n.251G=
NR_160740.1:n.2029G=
NR_160741.1:n.2029G=
NR_160742.1:n.2029G=
ENST00000311916.6:c.1423G=	ENSP00000309595.2:p.Ala475=
ENST00000370228.1:c.1423G=	ENSP00000359248.1:p.Ala475=
ENST00000370228.2:c.1423G=	ENSP00000359248.1:p.Ala475=
ENST00000459764.1:n.266G=
ENST00000473656.5:n.244G=
ENST00000476766.5:n.309G=
ENST00000643860.1:c.1423G=	ENSP00000494389.1:p.Ala475=
ENST00000646226.1:n.238G=
ENST00000647109.1:c.82G=
ENST00000650396.1:c.384G=
XM_011539974.1:c.61G=	XP_011538276.1:p.Ala21=
XM_011539975.1:c.61G=	XP_011538277.1:p.Ala21=
XM_011539975.2:c.61G=	XP_011538277.1:p.Ala21=
XM_017016437.1:c.61G=	XP_016871926.1:p.Ala21=
XR_001747142.1:n.1597G=
XR_001747144.1:n.1535G=
XR_002956991.1:n.1535G=
XR_945788.1:n.2194G=
XR_945788.2:n.1535G=