Canonical Allele Identifier: CA471184999

Gene: TWNK

Linked Data

• ClinVar Variation Id: 1640318
• ClinVar RCV Id: RCV002131662
• dbSNP Id: rs1483640254
• gnomAD v2: 10-102749603-C-T
• gnomAD v3: 10-100989846-C-T
• gnomAD v4: 10-100989846-C-T
• MyVariant Identifiers: chr10:g.102749603C>T (hg19) ; chr10:g.100989846C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100989846C>T , CM000672.2:g.100989846C>T	GRCh38
NC_000010.10:g.102749603C>T , CM000672.1:g.102749603C>T	GRCh37
NC_000010.9:g.102739593C>T	NCBI36
NG_011646.1:g.2670G>A
NG_012624.1:g.7311C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1446C>T MANE Select	ENSP00000309595.2:p.Pro482=
ENST00000370228.2:c.1446C>T	ENSP00000359248.1:p.Pro482=
ENST00000643860.1:c.1446C>T	ENSP00000494389.1:p.Pro482=
ENST00000646226.1:n.261C>T
ENST00000647109.1:c.105C>T
ENST00000650396.1:c.407C>T
ENST00000311916.6:c.1446C>T	ENSP00000309595.2:p.Pro482=
ENST00000370228.1:c.1446C>T	ENSP00000359248.1:p.Pro482=
ENST00000459764.1:n.289C>T
ENST00000473656.5:n.267C>T
ENST00000476766.5:n.332C>T
NM_001163812.1:c.1446C>T	NP_001157284.1:p.Pro482=
NM_001163813.1:c.84C>T	NP_001157285.1:p.Pro28=
NM_001163814.1:c.84C>T	NP_001157286.1:p.Pro28=
NM_021830.4:c.1446C>T	NP_068602.2:p.Pro482=
XM_011539974.1:c.84C>T	XP_011538276.1:p.Pro28=
XM_011539975.1:c.84C>T	XP_011538277.1:p.Pro28=
XR_945788.1:n.2217C>T
XM_011539975.2:c.84C>T	XP_011538277.1:p.Pro28=
XM_017016437.1:c.84C>T	XP_016871926.1:p.Pro28=
XR_001747142.1:n.1620C>T
XR_001747144.1:n.1558C>T
XR_002956991.1:n.1558C>T
XR_945788.2:n.1558C>T
NM_021830.5:c.1446C>T MANE Select	NP_068602.2:p.Pro482=
NM_001163812.2:c.1446C>T	NP_001157284.1:p.Pro482=
NM_001163813.2:c.84C>T	NP_001157285.1:p.Pro28=
NM_001163814.2:c.84C>T	NP_001157286.1:p.Pro28=
NM_001368275.1:c.84C>T	NP_001355204.1:p.Pro28=
NR_160738.1:n.2114C>T
NR_160739.1:n.274C>T
NR_160740.1:n.2052C>T
NR_160741.1:n.2052C>T
NR_160742.1:n.2052C>T