Canonical Allele Identifier: CA15876509

Gene: TAOK2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29977620A>G , CM000678.2:g.29977620A>G	GRCh38
NC_000016.9:g.29988941A>G , CM000678.1:g.29988941A>G	GRCh37
NC_000016.8:g.29896442A>G	NCBI36
NG_030462.1:g.8754A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308893.9:c.-35-118A>G MANE Select	ENSP00000310094.4:n.-35-118A>G
ENST00000279394.7:c.-35-118A>G	ENSP00000279394.3:n.-35-118A>G
ENST00000308893.8:c.-35-118A>G	ENSP00000310094.4:n.-35-118A>G
ENST00000543033.5:c.-35-118A>G	ENSP00000440336.1:n.-35-118A>G
NM_001252043.1:c.-35-118A>G	NP_001238972.1:n.-35-118A>G
NM_004783.3:c.-35-118A>G	NP_004774.1:n.-35-118A>G
NM_016151.3:c.-35-118A>G	NP_057235.2:n.-35-118A>G
XM_011545982.1:c.-35-118A>G	XP_011544284.1:n.-35-118A>G
XM_011545983.1:c.-35-118A>G	XP_011544285.1:n.-35-118A>G
XM_011545984.1:c.-35-118A>G	XP_011544286.1:n.-35-118A>G
XM_011545985.1:c.-35-118A>G	XP_011544287.1:n.-35-118A>G
XM_011545986.1:c.-35-118A>G	XP_011544288.1:n.-35-118A>G
XM_011545987.1:c.-35-118A>G	XP_011544289.1:n.-35-118A>G
XM_011545988.1:c.-35-118A>G	XP_011544290.1:n.-35-118A>G
XM_011545989.1:c.-35-118A>G	XP_011544291.1:n.-35-118A>G
XR_950873.1:n.1009-118A>G
XM_011545982.2:c.-35-118A>G	XP_011544284.1:n.-35-118A>G
XM_011545983.3:c.-35-118A>G	XP_011544285.1:n.-35-118A>G
XM_011545984.2:c.-35-118A>G	XP_011544286.1:n.-35-118A>G
XM_011545985.2:c.-35-118A>G	XP_011544287.1:n.-35-118A>G
XM_011545986.3:c.-35-118A>G	XP_011544288.1:n.-35-118A>G
XR_001752034.2:n.782-118A>G
XR_001752035.2:n.782-118A>G
XR_001752036.2:n.782-118A>G
XR_950873.2:n.782-118A>G
NM_016151.4:c.-35-118A>G MANE Select	NP_057235.2:n.-35-118A>G
NM_001252043.2:c.-35-118A>G	NP_001238972.1:n.-35-118A>G
NM_004783.4:c.-35-118A>G	NP_004774.1:n.-35-118A>G