Canonical Allele Identifier: CA5653086

Gene: TWNK

Linked Data

• ClinVar Variation Id: 2438448
• ClinVar RCV Id: RCV003139200
• dbSNP Id: rs146532064
• ExAC: 10:102748529 G / A
• gnomAD v2: 10-102748529-G-A
• gnomAD v3: 10-100988772-G-A
• gnomAD v4: 10-100988772-G-A
• MyVariant Identifiers: chr10:g.102748529G>A (hg19) ; chr10:g.100988772G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100988772G>A , CM000672.2:g.100988772G>A	GRCh38
NC_000010.10:g.102748529G>A , CM000672.1:g.102748529G>A	GRCh37
NC_000010.9:g.102738519G>A	NCBI36
NG_011646.1:g.3744C>T
NG_012624.1:g.6237G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311916.8:c.562G>A MANE Select	ENSP00000309595.2:p.Asp188Asn
ENST00000370228.2:c.562G>A	ENSP00000359248.1:p.Asp188Asn
ENST00000643860.1:c.562G>A	ENSP00000494389.1:p.Asp188Asn
ENST00000646226.1:n.59-872G>A
ENST00000311916.6:c.562G>A	ENSP00000309595.2:p.Asp188Asn
ENST00000370228.1:c.562G>A	ENSP00000359248.1:p.Asp188Asn
ENST00000459764.1:n.87-872G>A
ENST00000473656.5:n.65-872G>A
ENST00000476766.5:n.192-934G>A
NM_001163812.1:c.562G>A	NP_001157284.1:p.Asp188Asn
NM_001163813.1:c.-119-872G>A	NP_001157285.1:n.-119-872G>A
NM_001163814.1:c.-119-872G>A	NP_001157286.1:n.-119-872G>A
NM_021830.4:c.562G>A	NP_068602.2:p.Asp188Asn
XM_011539975.1:c.-57-934G>A	XP_011538277.1:n.-57-934G>A
XR_945788.1:n.1395G>A
XM_011539975.2:c.-57-934G>A	XP_011538277.1:n.-57-934G>A
XM_017016437.1:c.-739G>A	XP_016871926.1:n.-739G>A
XR_001747142.1:n.736G>A
XR_001747144.1:n.736G>A
XR_002956991.1:n.736G>A
XR_945788.2:n.736G>A
NM_021830.5:c.562G>A MANE Select	NP_068602.2:p.Asp188Asn
NM_001163812.2:c.562G>A	NP_001157284.1:p.Asp188Asn
NM_001163813.2:c.-119-872G>A	NP_001157285.1:n.-119-872G>A
NM_001163814.2:c.-119-872G>A	NP_001157286.1:n.-119-872G>A
NM_001368275.1:c.-57-934G>A	NP_001355204.1:n.-57-934G>A
NR_160738.1:n.1230G>A
NR_160739.1:n.72-872G>A
NR_160740.1:n.1230G>A
NR_160741.1:n.1230G>A
NR_160742.1:n.1230G>A