Canonical Allele Identifier: CA471268923

Gene: TWNK

Linked Data

• dbSNP Id: rs1851671742
• MyVariant Identifiers: chr10:g.102748630C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988873C>T , CM000672.2:g.100988873C>T	GRCh38
NC_000010.10:g.102748630C>T , CM000672.1:g.102748630C>T	GRCh37
NC_000010.9:g.102738620C>T	NCBI36
NG_011646.1:g.3643G>A
NG_012624.1:g.6338C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.663C>T MANE Select	ENSP00000309595.2:p.Leu221=
ENST00000370228.2:c.663C>T	ENSP00000359248.1:p.Leu221=
ENST00000643860.1:c.663C>T	ENSP00000494389.1:p.Leu221=
ENST00000646226.1:n.59-771C>T
ENST00000311916.6:c.663C>T	ENSP00000309595.2:p.Leu221=
ENST00000370228.1:c.663C>T	ENSP00000359248.1:p.Leu221=
ENST00000459764.1:n.87-771C>T
ENST00000473656.5:n.65-771C>T
ENST00000476766.5:n.192-833C>T
NM_001163812.1:c.663C>T	NP_001157284.1:p.Leu221=
NM_001163813.1:c.-119-771C>T	NP_001157285.1:n.-119-771C>T
NM_001163814.1:c.-119-771C>T	NP_001157286.1:n.-119-771C>T
NM_021830.4:c.663C>T	NP_068602.2:p.Leu221=
XM_011539975.1:c.-57-833C>T	XP_011538277.1:n.-57-833C>T
XR_945788.1:n.1496C>T
XM_011539975.2:c.-57-833C>T	XP_011538277.1:n.-57-833C>T
XM_017016437.1:c.-638C>T	XP_016871926.1:n.-638C>T
XR_001747142.1:n.837C>T
XR_001747144.1:n.837C>T
XR_002956991.1:n.837C>T
XR_945788.2:n.837C>T
NM_021830.5:c.663C>T MANE Select	NP_068602.2:p.Leu221=
NM_001163812.2:c.663C>T	NP_001157284.1:p.Leu221=
NM_001163813.2:c.-119-771C>T	NP_001157285.1:n.-119-771C>T
NM_001163814.2:c.-119-771C>T	NP_001157286.1:n.-119-771C>T
NM_001368275.1:c.-57-833C>T	NP_001355204.1:n.-57-833C>T
NR_160738.1:n.1331C>T
NR_160739.1:n.72-771C>T
NR_160740.1:n.1331C>T
NR_160741.1:n.1331C>T
NR_160742.1:n.1331C>T