Canonical Allele Identifier: CA2645131074
Gene: KCNQ4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40784142dup , CM000663.2:g.40784142dup GRCh38
NC_000001.10:g.41249814dup , CM000663.1:g.41249814dup GRCh37
NC_000001.9:g.41022401dup NCBI36
NG_008139.1:g.5131dup
NG_008139.2:g.5131dup
NG_008139.3:g.5356dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.49dup MANE Select ENSP00000262916.6:p.Asp17GlyfsTer?
ENST00000347132.9:c.49dup ENSP00000262916.6:p.Asp17GlyfsTer?
ENST00000509682.6:c.49dup ENSP00000423756.2:p.Asp17GlyfsTer?
NM_004700.3:c.49dup NP_004691.2:p.Asp17GlyfsTer?
NM_172163.2:c.49dup NP_751895.1:p.Asp17GlyfsTer?
XM_011542417.1:c.49dup XP_011540719.1:p.Asp17GlyfsTer?
XM_011542418.1:c.49dup XP_011540720.1:p.Asp17GlyfsTer?
XM_011542419.1:c.49dup XP_011540721.1:p.Asp17GlyfsTer?
XM_011542420.1:c.49dup XP_011540722.1:p.Asp17GlyfsTer?
XR_946798.1:n.55dup
XR_946799.1:n.55dup
XR_946800.1:n.55dup
NM_004700.4:c.49dup MANE Select NP_004691.2:p.Asp17GlyfsTer?
NM_172163.3:c.49dup NP_751895.1:p.Asp17GlyfsTer?