Canonical Allele Identifier: CA1164531223

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784351_40784360delinsGGTCTACAAC , CM000663.2:g.40784351_40784360delinsGGTCTACAAC	GRCh38
NC_000001.10:g.41250023_41250032delinsGGTCTACAAC , CM000663.1:g.41250023_41250032delinsGGTCTACAAC	GRCh37
NC_000001.9:g.41022610_41022619delinsGGTCTACAAC	NCBI36
NG_008139.1:g.5340_5349delinsGGTCTACAAC
NG_008139.2:g.5340_5349delinsGGTCTACAAC
NG_008139.3:g.5565_5574delinsGGTCTACAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.258_267delinsGGTCTACAAC MANE Select	ENSP00000262916.6:p.Trp86=
ENST00000347132.9:c.258_267delinsGGTCTACAAC	ENSP00000262916.6:p.Trp86=
ENST00000509682.6:c.258_267delinsGGTCTACAAC	ENSP00000423756.2:p.Trp86=
NM_004700.3:c.258_267delinsGGTCTACAAC	NP_004691.2:p.Trp86=
NM_172163.2:c.258_267delinsGGTCTACAAC	NP_751895.1:p.Trp86=
XM_011542417.1:c.258_267delinsGGTCTACAAC	XP_011540719.1:p.Trp86=
XM_011542418.1:c.258_267delinsGGTCTACAAC	XP_011540720.1:p.Trp86=
XM_011542419.1:c.258_267delinsGGTCTACAAC	XP_011540721.1:p.Trp86=
XM_011542420.1:c.258_267delinsGGTCTACAAC	XP_011540722.1:p.Trp86=
XR_946798.1:n.264_273delinsGGTCTACAAC
XR_946799.1:n.264_273delinsGGTCTACAAC
XR_946800.1:n.264_273delinsGGTCTACAAC
NM_004700.4:c.258_267delinsGGTCTACAAC MANE Select	NP_004691.2:p.Trp86=
NM_172163.3:c.258_267delinsGGTCTACAAC	NP_751895.1:p.Trp86=