Canonical Allele Identifier: CA212964024

Gene: TWNK

Linked Data

• dbSNP Id: rs1052916175
• gnomAD v3: 10-100990727-G-C
• gnomAD v4: 10-100990727-G-C
• MyVariant Identifiers: chr10:g.102750484G>C (hg19) ; chr10:g.100990727G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100990727G>C , CM000672.2:g.100990727G>C	GRCh38
NC_000010.10:g.102750484G>C , CM000672.1:g.102750484G>C	GRCh37
NC_000010.9:g.102740474G>C	NCBI36
NG_011646.1:g.1789C>G
NG_012624.1:g.8192G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.1593-142G>C MANE Select	ENSP00000309595.2:n.1593-142G>C
ENST00000370228.2:c.1593-142G>C	ENSP00000359248.1:n.1593-142G>C
ENST00000643860.1:c.*116+64G>C	ENSP00000494389.1:n.*116+64G>C
ENST00000646226.1:n.408-142G>C
ENST00000647109.1:c.252-142G>C
ENST00000650396.1:c.673+64G>C
ENST00000311916.6:c.1593-142G>C	ENSP00000309595.2:n.1593-142G>C
ENST00000370228.1:c.1593-142G>C	ENSP00000359248.1:n.1593-142G>C
ENST00000473656.5:n.414-142G>C
ENST00000476766.5:n.479-142G>C
NM_001163812.1:c.1593-142G>C	NP_001157284.1:n.1593-142G>C
NM_001163813.1:c.231-142G>C	NP_001157285.1:n.231-142G>C
NM_001163814.1:c.231-142G>C	NP_001157286.1:n.231-142G>C
NM_021830.4:c.1593-142G>C	NP_068602.2:n.1593-142G>C
XM_011539974.1:c.231-142G>C	XP_011538276.1:n.231-142G>C
XM_011539975.1:c.231-142G>C	XP_011538277.1:n.231-142G>C
XR_945788.1:n.2364-142G>C
XM_011539975.2:c.231-142G>C	XP_011538277.1:n.231-142G>C
XM_017016437.1:c.231-142G>C	XP_016871926.1:n.231-142G>C
XR_001747142.1:n.1886+64G>C
XR_001747144.1:n.1824+64G>C
XR_002956991.1:n.1705-142G>C
XR_945788.2:n.1705-142G>C
NM_021830.5:c.1593-142G>C MANE Select	NP_068602.2:n.1593-142G>C
NM_001163812.2:c.1593-142G>C	NP_001157284.1:n.1593-142G>C
NM_001163813.2:c.231-142G>C	NP_001157285.1:n.231-142G>C
NM_001163814.2:c.231-142G>C	NP_001157286.1:n.231-142G>C
NM_001368275.1:c.231-142G>C	NP_001355204.1:n.231-142G>C
NR_160738.1:n.2380+64G>C
NR_160739.1:n.540+64G>C
NR_160740.1:n.2199-142G>C
NR_160741.1:n.2199-142G>C
NR_160742.1:n.2318+64G>C