Canonical Allele Identifier: CA471268734

Gene: TWNK

Linked Data

• MyVariant Identifiers: chr10:g.102748363A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988606A>G , CM000672.2:g.100988606A>G	GRCh38
NC_000010.10:g.102748363A>G , CM000672.1:g.102748363A>G	GRCh37
NC_000010.9:g.102738353A>G	NCBI36
NG_011646.1:g.3910T>C
NG_012624.1:g.6071A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.396A>G MANE Select	ENSP00000309595.2:p.Arg132=
ENST00000370228.2:c.396A>G	ENSP00000359248.1:p.Arg132=
ENST00000643860.1:c.396A>G	ENSP00000494389.1:p.Arg132=
ENST00000646226.1:n.58+993A>G
ENST00000311916.6:c.396A>G	ENSP00000309595.2:p.Arg132=
ENST00000370228.1:c.396A>G	ENSP00000359248.1:p.Arg132=
ENST00000459764.1:n.86+726A>G
ENST00000473656.5:n.64+993A>G
ENST00000476766.5:n.191+1049A>G
NM_001163812.1:c.396A>G	NP_001157284.1:p.Arg132=
NM_001163813.1:c.-120+993A>G	NP_001157285.1:n.-120+993A>G
NM_001163814.1:c.-120+993A>G	NP_001157286.1:n.-120+993A>G
NM_021830.4:c.396A>G	NP_068602.2:p.Arg132=
XM_011539975.1:c.-58+993A>G	XP_011538277.1:n.-58+993A>G
XR_945788.1:n.1229A>G
XM_011539975.2:c.-58+993A>G	XP_011538277.1:n.-58+993A>G
XM_017016437.1:c.-905A>G	XP_016871926.1:n.-905A>G
XR_001747142.1:n.570A>G
XR_001747144.1:n.570A>G
XR_002956991.1:n.570A>G
XR_945788.2:n.570A>G
NM_021830.5:c.396A>G MANE Select	NP_068602.2:p.Arg132=
NM_001163812.2:c.396A>G	NP_001157284.1:p.Arg132=
NM_001163813.2:c.-120+993A>G	NP_001157285.1:n.-120+993A>G
NM_001163814.2:c.-120+993A>G	NP_001157286.1:n.-120+993A>G
NM_001368275.1:c.-58+993A>G	NP_001355204.1:n.-58+993A>G
NR_160738.1:n.1064A>G
NR_160739.1:n.71+993A>G
NR_160740.1:n.1064A>G
NR_160741.1:n.1064A>G
NR_160742.1:n.1064A>G