Canonical Allele Identifier: CA366480861

Gene: QKI

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.163562071T>C , CM000668.2:g.163562071T>C	GRCh38
NC_000006.11:g.163983103T>C , CM000668.1:g.163983103T>C	GRCh37
NC_000006.10:g.163903093T>C	NCBI36
NG_029604.1:g.152429T>C
NG_029604.2:g.152429T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361752.8:c.634+2T>C MANE Select	ENSP00000355094.3:n.634+2T>C
ENST00000275262.11:c.634+2T>C	ENSP00000275262.7:n.634+2T>C
ENST00000361195.6:c.634+2T>C	ENSP00000354867.2:n.634+2T>C
ENST00000361752.7:c.634+2T>C	ENSP00000355094.3:n.634+2T>C
ENST00000361758.8:c.634+2T>C	ENSP00000354951.4:n.634+2T>C
ENST00000392127.6:c.634+2T>C	ENSP00000375973.2:n.634+2T>C
ENST00000424802.7:c.634+2T>C	ENSP00000408382.3:n.634+2T>C
ENST00000453779.6:c.634+2T>C	ENSP00000408775.2:n.634+2T>C
ENST00000537041.5:c.469+2T>C	ENSP00000440991.1:n.469+2T>C
ENST00000537883.5:c.323+2T>C
ENST00000540719.1:n.255+2T>C
ENST00000544361.1:c.134+2T>C
ENST00000544823.5:c.469+2T>C	ENSP00000440599.1:n.469+2T>C
ENST00000545607.5:c.447+2T>C
NM_001301085.1:c.634+2T>C	NP_001288014.1:n.634+2T>C
NM_006775.2:c.634+2T>C	NP_006766.1:n.634+2T>C
NM_206853.2:c.634+2T>C	NP_996735.1:n.634+2T>C
NM_206854.2:c.634+2T>C	NP_996736.1:n.634+2T>C
NM_206855.2:c.634+2T>C	NP_996737.1:n.634+2T>C
XM_011536258.1:c.634+2T>C	XP_011534560.1:n.634+2T>C
XM_011536259.1:c.634+2T>C	XP_011534561.1:n.634+2T>C
XM_011536260.1:c.490+2T>C	XP_011534562.1:n.490+2T>C
XR_245557.2:n.692+2T>C
XR_942633.1:n.692+2T>C
XM_011536258.2:c.634+2T>C	XP_011534560.1:n.634+2T>C
XM_011536259.2:c.634+2T>C	XP_011534561.1:n.634+2T>C
XM_011536260.2:c.490+2T>C	XP_011534562.1:n.490+2T>C
XM_017011502.1:c.634+2T>C	XP_016866991.1:n.634+2T>C
XM_017011503.1:c.634+2T>C	XP_016866992.1:n.634+2T>C
XM_017011504.1:c.634+2T>C	XP_016866993.1:n.634+2T>C
XR_001743749.1:n.1342+2T>C
XR_001743750.1:n.692+2T>C
XR_245557.3:n.692+2T>C
XR_942633.2:n.692+2T>C
NM_006775.3:c.634+2T>C MANE Select	NP_006766.1:n.634+2T>C
NM_001301085.2:c.634+2T>C	NP_001288014.1:n.634+2T>C
NM_206853.3:c.634+2T>C	NP_996735.1:n.634+2T>C
NM_206854.3:c.634+2T>C	NP_996736.1:n.634+2T>C
NM_206855.3:c.634+2T>C	NP_996737.1:n.634+2T>C