Canonical Allele Identifier: CA1932019342

Gene: TWNK

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988885A= , CM000672.2:g.100988885A=	GRCh38
NC_000010.10:g.102748642A= , CM000672.1:g.102748642A=	GRCh37
NC_000010.9:g.102738632A=	NCBI36
NG_011646.1:g.3631T=
NG_012624.1:g.6350A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.675A= MANE Select	ENSP00000309595.2:p.Lys225=
ENST00000370228.2:c.675A=	ENSP00000359248.1:p.Lys225=
ENST00000643860.1:c.675A=	ENSP00000494389.1:p.Lys225=
ENST00000646226.1:n.59-759A=
ENST00000311916.6:c.675A=	ENSP00000309595.2:p.Lys225=
ENST00000370228.1:c.675A=	ENSP00000359248.1:p.Lys225=
ENST00000459764.1:n.87-759A=
ENST00000473656.5:n.65-759A=
ENST00000476766.5:n.192-821A=
NM_001163812.1:c.675A=	NP_001157284.1:p.Lys225=
NM_001163813.1:c.-119-759A=	NP_001157285.1:n.-119-759A=
NM_001163814.1:c.-119-759A=	NP_001157286.1:n.-119-759A=
NM_021830.4:c.675A=	NP_068602.2:p.Lys225=
XM_011539975.1:c.-57-821A=	XP_011538277.1:n.-57-821A=
XR_945788.1:n.1508A=
XM_011539975.2:c.-57-821A=	XP_011538277.1:n.-57-821A=
XM_017016437.1:c.-626A=	XP_016871926.1:n.-626A=
XR_001747142.1:n.849A=
XR_001747144.1:n.849A=
XR_002956991.1:n.849A=
XR_945788.2:n.849A=
NM_021830.5:c.675A= MANE Select	NP_068602.2:p.Lys225=
NM_001163812.2:c.675A=	NP_001157284.1:p.Lys225=
NM_001163813.2:c.-119-759A=	NP_001157285.1:n.-119-759A=
NM_001163814.2:c.-119-759A=	NP_001157286.1:n.-119-759A=
NM_001368275.1:c.-57-821A=	NP_001355204.1:n.-57-821A=
NR_160738.1:n.1343A=
NR_160739.1:n.72-759A=
NR_160740.1:n.1343A=
NR_160741.1:n.1343A=
NR_160742.1:n.1343A=