Canonical Allele Identifier: CA372290487

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133187788A>G (hg19) ; chr8:g.132175541A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175541A>G , CM000670.2:g.132175541A>G	GRCh38
NC_000008.10:g.133187788A>G , CM000670.1:g.133187788A>G	GRCh37
NC_000008.9:g.133256970A>G	NCBI36
NG_008854.2:g.310217T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.845T>C MANE Select	ENSP00000373648.3:p.Val282Ala
ENST00000521134.6:c.485T>C	ENSP00000429799.1:p.Val162Ala
ENST00000638588.1:c.518T>C	ENSP00000491940.1:p.Val173Ala
ENST00000639358.1:c.495T>C
ENST00000639496.1:c.518T>C	ENSP00000491165.1:p.Val173Ala
ENST00000388996.8:c.845T>C	ENSP00000373648.3:p.Val282Ala
ENST00000519445.5:c.845T>C	ENSP00000428790.1:p.Val282Ala
ENST00000519589.1:n.623T>C
ENST00000521134.5:c.485T>C	ENSP00000429799.1:p.Val162Ala
ENST00000621976.1:c.482T>C	ENSP00000482510.1:p.Val161Ala
NM_001204824.1:c.485T>C	NP_001191753.1:p.Val162Ala
NM_004519.3:c.845T>C	NP_004510.1:p.Val282Ala
XM_005250914.2:c.-312T>C	XP_005250971.1:n.-312T>C
XM_006716555.2:c.137T>C	XP_006716618.1:p.Val46Ala
XM_011517026.1:c.485T>C	XP_011515328.1:p.Val162Ala
XM_005250914.3:c.-312T>C	XP_005250971.1:n.-312T>C
XM_006716555.3:c.137T>C	XP_006716618.1:p.Val46Ala
XM_011517026.2:c.485T>C	XP_011515328.1:p.Val162Ala
XM_017013400.1:c.623T>C	XP_016868889.1:p.Val208Ala
NM_004519.4:c.845T>C MANE Select	NP_004510.1:p.Val282Ala
NM_001204824.2:c.485T>C	NP_001191753.1:p.Val162Ala