Canonical Allele Identifier: CA2645131306

Gene: KCNQ4

Linked Data

• gnomAD v4: 1-40784197-AGGCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784204_40784207del , CM000663.2:g.40784204_40784207del	GRCh38
NC_000001.10:g.41249876_41249879del , CM000663.1:g.41249876_41249879del	GRCh37
NC_000001.9:g.41022463_41022466del	NCBI36
NG_008139.1:g.5193_5196del
NG_008139.2:g.5193_5196del
NG_008139.3:g.5418_5421del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.111_114del MANE Select	ENSP00000262916.6:p.Gly38AlafsTer?
ENST00000347132.9:c.111_114del	ENSP00000262916.6:p.Gly38AlafsTer?
ENST00000509682.6:c.111_114del	ENSP00000423756.2:p.Gly38AlafsTer?
NM_004700.3:c.111_114del	NP_004691.2:p.Gly38AlafsTer?
NM_172163.2:c.111_114del	NP_751895.1:p.Gly38AlafsTer?
XM_011542417.1:c.111_114del	XP_011540719.1:p.Gly38AlafsTer?
XM_011542418.1:c.111_114del	XP_011540720.1:p.Gly38AlafsTer?
XM_011542419.1:c.111_114del	XP_011540721.1:p.Gly38AlafsTer?
XM_011542420.1:c.111_114del	XP_011540722.1:p.Gly38AlafsTer?
XR_946798.1:n.117_120del
XR_946799.1:n.117_120del
XR_946800.1:n.117_120del
NM_004700.4:c.111_114del MANE Select	NP_004691.2:p.Gly38AlafsTer?
NM_172163.3:c.111_114del	NP_751895.1:p.Gly38AlafsTer?