Canonical Allele Identifier: CA1820664457

Gene: KCNQ3

Linked Data

• dbSNP Id: rs1826510995

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175316del , CM000670.2:g.132175316del	GRCh38
NC_000008.10:g.133187563del , CM000670.1:g.133187563del	GRCh37
NC_000008.9:g.133256745del	NCBI36
NG_008854.2:g.310442del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.933+137del MANE Select	ENSP00000373648.3:n.933+137del
ENST00000521134.6:c.573+137del	ENSP00000429799.1:n.573+137del
ENST00000638588.1:c.606+137del	ENSP00000491940.1:n.606+137del
ENST00000639358.1:c.583+137del
ENST00000639496.1:c.606+137del	ENSP00000491165.1:n.606+137del
ENST00000388996.8:c.933+137del	ENSP00000373648.3:n.933+137del
ENST00000519445.5:c.933+137del	ENSP00000428790.1:n.933+137del
ENST00000519589.1:n.711+137del
ENST00000521134.5:c.573+137del	ENSP00000429799.1:n.573+137del
ENST00000621976.1:c.570+137del	ENSP00000482510.1:n.570+137del
NM_001204824.1:c.573+137del	NP_001191753.1:n.573+137del
NM_004519.3:c.933+137del	NP_004510.1:n.933+137del
XM_005250914.2:c.-224+137del	XP_005250971.1:n.-224+137del
XM_006716555.2:c.225+137del	XP_006716618.1:n.225+137del
XM_011517026.1:c.573+137del	XP_011515328.1:n.573+137del
XM_005250914.3:c.-224+137del	XP_005250971.1:n.-224+137del
XM_006716555.3:c.225+137del	XP_006716618.1:n.225+137del
XM_011517026.2:c.573+137del	XP_011515328.1:n.573+137del
XM_017013400.1:c.711+137del	XP_016868889.1:n.711+137del
NM_004519.4:c.933+137del MANE Select	NP_004510.1:n.933+137del
NM_001204824.2:c.573+137del	NP_001191753.1:n.573+137del