Canonical Allele Identifier: CA2743311932

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40831070_40831071insA , CM000663.2:g.40831070_40831071insA	GRCh38
NC_000001.10:g.41296742_41296743insA , CM000663.1:g.41296742_41296743insA	GRCh37
NC_000001.9:g.41069329_41069330insA	NCBI36
NG_008139.1:g.52059_52060insA
NG_008139.2:g.52059_52060insA
NG_008139.3:g.52284_52285insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.1293-14_1293-13insA MANE Select	ENSP00000262916.6:n.1293-14_1293-13insA
ENST00000347132.9:c.1293-14_1293-13insA	ENSP00000262916.6:n.1293-14_1293-13insA
ENST00000443478.3:c.874-14_874-13insA
ENST00000506017.1:n.612-14_612-13insA
ENST00000509682.6:c.1131-14_1131-13insA	ENSP00000423756.2:n.1131-14_1131-13insA
NM_004700.3:c.1293-14_1293-13insA	NP_004691.2:n.1293-14_1293-13insA
NM_172163.2:c.1131-14_1131-13insA	NP_751895.1:n.1131-14_1131-13insA
XM_011542418.1:c.*223_*224insA	XP_011540720.1:n.*223_*224insA
XR_946798.1:n.1299-14_1299-13insA
XR_946799.1:n.1299-14_1299-13insA
XR_946800.1:n.1048-14_1048-13insA
XM_017002792.1:c.276-14_276-13insA	XP_016858281.1:n.276-14_276-13insA
NM_004700.4:c.1293-14_1293-13insA MANE Select	NP_004691.2:n.1293-14_1293-13insA
NM_172163.3:c.1131-14_1131-13insA	NP_751895.1:n.1131-14_1131-13insA