Canonical Allele Identifier: CA372290544

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133187815A>G (hg19) ; chr8:g.132175568A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175568A>G , CM000670.2:g.132175568A>G	GRCh38
NC_000008.10:g.133187815A>G , CM000670.1:g.133187815A>G	GRCh37
NC_000008.9:g.133256997A>G	NCBI36
NG_008854.2:g.310190T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.818T>C MANE Select	ENSP00000373648.3:p.Ile273Thr
ENST00000521134.6:c.458T>C	ENSP00000429799.1:p.Ile153Thr
ENST00000638588.1:c.491T>C	ENSP00000491940.1:p.Ile164Thr
ENST00000639358.1:c.468T>C
ENST00000639496.1:c.491T>C	ENSP00000491165.1:p.Ile164Thr
ENST00000388996.8:c.818T>C	ENSP00000373648.3:p.Ile273Thr
ENST00000519445.5:c.818T>C	ENSP00000428790.1:p.Ile273Thr
ENST00000519589.1:n.596T>C
ENST00000521134.5:c.458T>C	ENSP00000429799.1:p.Ile153Thr
ENST00000621976.1:c.455T>C	ENSP00000482510.1:p.Ile152Thr
NM_001204824.1:c.458T>C	NP_001191753.1:p.Ile153Thr
NM_004519.3:c.818T>C	NP_004510.1:p.Ile273Thr
XM_005250914.2:c.-339T>C	XP_005250971.1:n.-339T>C
XM_006716555.2:c.110T>C	XP_006716618.1:p.Ile37Thr
XM_011517026.1:c.458T>C	XP_011515328.1:p.Ile153Thr
XM_005250914.3:c.-339T>C	XP_005250971.1:n.-339T>C
XM_006716555.3:c.110T>C	XP_006716618.1:p.Ile37Thr
XM_011517026.2:c.458T>C	XP_011515328.1:p.Ile153Thr
XM_017013400.1:c.596T>C	XP_016868889.1:p.Ile199Thr
NM_004519.4:c.818T>C MANE Select	NP_004510.1:p.Ile273Thr
NM_001204824.2:c.458T>C	NP_001191753.1:p.Ile153Thr