Canonical Allele Identifier: CA1000909552
Gene: KCNQ4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40784202_40784203insC , CM000663.2:g.40784202_40784203insC GRCh38
NC_000001.10:g.41249874_41249875insC , CM000663.1:g.41249874_41249875insC GRCh37
NC_000001.9:g.41022461_41022462insC NCBI36
NG_008139.1:g.5191_5192insC
NG_008139.2:g.5191_5192insC
NG_008139.3:g.5416_5417insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.109_110insC MANE Select ENSP00000262916.6:p.Gly37AlafsTer?
ENST00000347132.9:c.109_110insC ENSP00000262916.6:p.Gly37AlafsTer?
ENST00000509682.6:c.109_110insC ENSP00000423756.2:p.Gly37AlafsTer?
NM_004700.3:c.109_110insC NP_004691.2:p.Gly37AlafsTer?
NM_172163.2:c.109_110insC NP_751895.1:p.Gly37AlafsTer?
XM_011542417.1:c.109_110insC XP_011540719.1:p.Gly37AlafsTer?
XM_011542418.1:c.109_110insC XP_011540720.1:p.Gly37AlafsTer?
XM_011542419.1:c.109_110insC XP_011540721.1:p.Gly37AlafsTer?
XM_011542420.1:c.109_110insC XP_011540722.1:p.Gly37AlafsTer?
XR_946798.1:n.115_116insC
XR_946799.1:n.115_116insC
XR_946800.1:n.115_116insC
NM_004700.4:c.109_110insC MANE Select NP_004691.2:p.Gly37AlafsTer?
NM_172163.3:c.109_110insC NP_751895.1:p.Gly37AlafsTer?