Canonical Allele Identifier: CA13730266

Gene: TAOK3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.118152057T>C , CM000674.2:g.118152057T>C	GRCh38
NC_000012.11:g.118589862T>C , CM000674.1:g.118589862T>C	GRCh37
NC_000012.10:g.117074245T>C	NCBI36
NG_051835.1:g.225889A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392533.8:c.2535+170A>G MANE Select	ENSP00000376317.3:n.2535+170A>G
ENST00000392533.7:c.2535+170A>G	ENSP00000376317.3:n.2535+170A>G
ENST00000419821.6:c.2535+170A>G	ENSP00000416374.2:n.2535+170A>G
ENST00000536979.1:c.120+170A>G	ENSP00000441932.1:n.120+170A>G
ENST00000537305.5:n.3216+170A>G
ENST00000537952.1:c.1155+170A>G	ENSP00000443834.1:n.1155+170A>G
ENST00000543709.5:n.396+170A>G
NM_016281.3:c.2535+170A>G	NP_057365.3:n.2535+170A>G
XM_005253897.1:c.2562+170A>G	XP_005253954.1:n.2562+170A>G
XM_005253898.1:c.2562+170A>G	XP_005253955.1:n.2562+170A>G
XM_006719445.2:c.2562+170A>G	XP_006719508.1:n.2562+170A>G
XM_006719446.2:c.2563-62A>G	XP_006719509.1:n.2563-62A>G
XM_011538437.1:c.2562+170A>G	XP_011536739.1:n.2562+170A>G
XM_011538438.1:c.2562+170A>G	XP_011536740.1:n.2562+170A>G
XM_011538439.1:c.2535+170A>G	XP_011536741.1:n.2535+170A>G
XM_011538440.1:c.2052+170A>G	XP_011536742.1:n.2052+170A>G
NM_001346487.1:c.2562+170A>G	NP_001333416.1:n.2562+170A>G
NM_001346488.1:c.2535+170A>G	NP_001333417.1:n.2535+170A>G
NM_001346489.1:c.2535+170A>G	NP_001333418.1:n.2535+170A>G
NM_001346490.1:c.2052+170A>G	NP_001333419.1:n.2052+170A>G
NM_001346491.1:c.2025+170A>G	NP_001333420.1:n.2025+170A>G
NM_001346492.1:c.2025+170A>G	NP_001333421.1:n.2025+170A>G
NM_001346493.1:c.2025+170A>G	NP_001333422.1:n.2025+170A>G
NM_001346494.1:c.1155+170A>G	NP_001333423.1:n.1155+170A>G
NM_001346495.1:c.1155+170A>G	NP_001333424.1:n.1155+170A>G
NM_001346496.1:c.1155+170A>G	NP_001333425.1:n.1155+170A>G
NM_001346497.1:c.1155+170A>G	NP_001333426.1:n.1155+170A>G
XM_005253898.2:c.2562+170A>G	XP_005253955.1:n.2562+170A>G
XM_006719445.3:c.2562+170A>G	XP_006719508.1:n.2562+170A>G
XM_011538437.2:c.2562+170A>G	XP_011536739.1:n.2562+170A>G
XM_017019408.2:c.2562+170A>G	XP_016874897.1:n.2562+170A>G
XM_017019409.2:c.2562+170A>G	XP_016874898.1:n.2562+170A>G
XM_017019410.2:c.2562+170A>G	XP_016874899.1:n.2562+170A>G
XM_017019412.2:c.2052+170A>G	XP_016874901.1:n.2052+170A>G
XM_017019413.2:c.2025+170A>G	XP_016874902.1:n.2025+170A>G
XM_024449010.1:c.2562+170A>G	XP_024304778.1:n.2562+170A>G
NM_016281.4:c.2535+170A>G MANE Select	NP_057365.3:n.2535+170A>G
NM_001346487.2:c.2562+170A>G	NP_001333416.1:n.2562+170A>G
NM_001346488.2:c.2535+170A>G	NP_001333417.1:n.2535+170A>G
NM_001346489.2:c.2535+170A>G	NP_001333418.1:n.2535+170A>G
NM_001346490.2:c.2052+170A>G	NP_001333419.1:n.2052+170A>G
NM_001346491.2:c.2025+170A>G	NP_001333420.1:n.2025+170A>G
NM_001346492.2:c.2025+170A>G	NP_001333421.1:n.2025+170A>G
NM_001346493.2:c.2025+170A>G	NP_001333422.1:n.2025+170A>G
NM_001346494.2:c.1155+170A>G	NP_001333423.1:n.1155+170A>G
NM_001346495.2:c.1155+170A>G	NP_001333424.1:n.1155+170A>G
NM_001346496.2:c.1155+170A>G	NP_001333425.1:n.1155+170A>G
NM_001346497.2:c.1155+170A>G	NP_001333426.1:n.1155+170A>G