Canonical Allele Identifier: CA372290398

Gene: KCNQ3

Linked Data

• gnomAD v4: 8-132175500-T-C
• MyVariant Identifiers: chr8:g.133187747T>C (hg19) ; chr8:g.132175500T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175500T>C , CM000670.2:g.132175500T>C	GRCh38
NC_000008.10:g.133187747T>C , CM000670.1:g.133187747T>C	GRCh37
NC_000008.9:g.133256929T>C	NCBI36
NG_008854.2:g.310258A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.886A>G MANE Select	ENSP00000373648.3:p.Met296Val
ENST00000521134.6:c.526A>G	ENSP00000429799.1:p.Met176Val
ENST00000638588.1:c.559A>G	ENSP00000491940.1:p.Met187Val
ENST00000639358.1:c.536A>G
ENST00000639496.1:c.559A>G	ENSP00000491165.1:p.Met187Val
ENST00000388996.8:c.886A>G	ENSP00000373648.3:p.Met296Val
ENST00000519445.5:c.886A>G	ENSP00000428790.1:p.Met296Val
ENST00000519589.1:n.664A>G
ENST00000521134.5:c.526A>G	ENSP00000429799.1:p.Met176Val
ENST00000621976.1:c.523A>G	ENSP00000482510.1:p.Met175Val
NM_001204824.1:c.526A>G	NP_001191753.1:p.Met176Val
NM_004519.3:c.886A>G	NP_004510.1:p.Met296Val
XM_005250914.2:c.-271A>G	XP_005250971.1:n.-271A>G
XM_006716555.2:c.178A>G	XP_006716618.1:p.Met60Val
XM_011517026.1:c.526A>G	XP_011515328.1:p.Met176Val
XM_005250914.3:c.-271A>G	XP_005250971.1:n.-271A>G
XM_006716555.3:c.178A>G	XP_006716618.1:p.Met60Val
XM_011517026.2:c.526A>G	XP_011515328.1:p.Met176Val
XM_017013400.1:c.664A>G	XP_016868889.1:p.Met222Val
NM_004519.4:c.886A>G MANE Select	NP_004510.1:p.Met296Val
NM_001204824.2:c.526A>G	NP_001191753.1:p.Met176Val