Canonical Allele Identifier: CA10630250

Gene: KCNQ3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132128103C>T , CM000670.2:g.132128103C>T	GRCh38
NC_000008.10:g.133140350C>T , CM000670.1:g.133140350C>T	GRCh37
NC_000008.9:g.133209532C>T	NCBI36
NG_008854.2:g.357655G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.*1159G>A MANE Select	ENSP00000373648.3:n.*1159G>A
ENST00000639496.1:c.*2402G>A	ENSP00000491165.1:n.*2402G>A
ENST00000388996.8:c.*1159G>A	ENSP00000373648.3:n.*1159G>A
ENST00000621976.1:c.3415G>A	ENSP00000482510.1:n.3415G>A
NM_001204824.1:c.*1159G>A	NP_001191753.1:n.*1159G>A
NM_004519.3:c.*1159G>A	NP_004510.1:n.*1159G>A
XM_005250914.2:c.*1159G>A	XP_005250971.1:n.*1159G>A
XM_006716555.2:c.*1159G>A	XP_006716618.1:n.*1159G>A
XM_011517026.1:c.*1159G>A	XP_011515328.1:n.*1159G>A
XM_005250914.3:c.*1159G>A	XP_005250971.1:n.*1159G>A
XM_006716555.3:c.*1159G>A	XP_006716618.1:n.*1159G>A
XM_011517026.2:c.*1159G>A	XP_011515328.1:n.*1159G>A
XM_017013400.1:c.*1159G>A	XP_016868889.1:n.*1159G>A
NM_004519.4:c.*1159G>A MANE Select	NP_004510.1:n.*1159G>A
NM_001204824.2:c.*1159G>A	NP_001191753.1:n.*1159G>A