Canonical Allele Identifier: CA378210968

Gene: TWNK

Linked Data

• MyVariant Identifiers: chr10:g.102749622C>A (hg19) ; chr10:g.100989865C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989865C>A , CM000672.2:g.100989865C>A	GRCh38
NC_000010.10:g.102749622C>A , CM000672.1:g.102749622C>A	GRCh37
NC_000010.9:g.102739612C>A	NCBI36
NG_011646.1:g.2651G>T
NG_012624.1:g.7330C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1465C>A MANE Select	ENSP00000309595.2:p.His489Asn
ENST00000370228.2:c.1465C>A	ENSP00000359248.1:p.His489Asn
ENST00000643860.1:c.1465C>A	ENSP00000494389.1:p.His489Asn
ENST00000646226.1:n.280C>A
ENST00000647109.1:c.124C>A
ENST00000650396.1:c.426C>A
ENST00000311916.6:c.1465C>A	ENSP00000309595.2:p.His489Asn
ENST00000370228.1:c.1465C>A	ENSP00000359248.1:p.His489Asn
ENST00000459764.1:n.308C>A
ENST00000473656.5:n.286C>A
ENST00000476766.5:n.351C>A
NM_001163812.1:c.1465C>A	NP_001157284.1:p.His489Asn
NM_001163813.1:c.103C>A	NP_001157285.1:p.His35Asn
NM_001163814.1:c.103C>A	NP_001157286.1:p.His35Asn
NM_021830.4:c.1465C>A	NP_068602.2:p.His489Asn
XM_011539974.1:c.103C>A	XP_011538276.1:p.His35Asn
XM_011539975.1:c.103C>A	XP_011538277.1:p.His35Asn
XR_945788.1:n.2236C>A
XM_011539975.2:c.103C>A	XP_011538277.1:p.His35Asn
XM_017016437.1:c.103C>A	XP_016871926.1:p.His35Asn
XR_001747142.1:n.1639C>A
XR_001747144.1:n.1577C>A
XR_002956991.1:n.1577C>A
XR_945788.2:n.1577C>A
NM_021830.5:c.1465C>A MANE Select	NP_068602.2:p.His489Asn
NM_001163812.2:c.1465C>A	NP_001157284.1:p.His489Asn
NM_001163813.2:c.103C>A	NP_001157285.1:p.His35Asn
NM_001163814.2:c.103C>A	NP_001157286.1:p.His35Asn
NM_001368275.1:c.103C>A	NP_001355204.1:p.His35Asn
NR_160738.1:n.2133C>A
NR_160739.1:n.293C>A
NR_160740.1:n.2071C>A
NR_160741.1:n.2071C>A
NR_160742.1:n.2071C>A