Canonical Allele Identifier: CA2574332531

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784124_40784125insA , CM000663.2:g.40784124_40784125insA	GRCh38
NC_000001.10:g.41249796_41249797insA , CM000663.1:g.41249796_41249797insA	GRCh37
NC_000001.9:g.41022383_41022384insA	NCBI36
NG_008139.1:g.5113_5114insA
NG_008139.2:g.5113_5114insA
NG_008139.3:g.5338_5339insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.31_32insA MANE Select	ENSP00000262916.6:p.Leu11HisfsTer?
ENST00000347132.9:c.31_32insA	ENSP00000262916.6:p.Leu11HisfsTer?
ENST00000509682.6:c.31_32insA	ENSP00000423756.2:p.Leu11HisfsTer?
NM_004700.3:c.31_32insA	NP_004691.2:p.Leu11HisfsTer?
NM_172163.2:c.31_32insA	NP_751895.1:p.Leu11HisfsTer?
XM_011542417.1:c.31_32insA	XP_011540719.1:p.Leu11HisfsTer?
XM_011542418.1:c.31_32insA	XP_011540720.1:p.Leu11HisfsTer?
XM_011542419.1:c.31_32insA	XP_011540721.1:p.Leu11HisfsTer?
XM_011542420.1:c.31_32insA	XP_011540722.1:p.Leu11HisfsTer?
XR_946798.1:n.37_38insA
XR_946799.1:n.37_38insA
XR_946800.1:n.37_38insA
NM_004700.4:c.31_32insA MANE Select	NP_004691.2:p.Leu11HisfsTer?
NM_172163.3:c.31_32insA	NP_751895.1:p.Leu11HisfsTer?