Canonical Allele Identifier: CA1164531029
Gene: KCNQ4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40784042C= , CM000663.2:g.40784042C= GRCh38
NC_000001.10:g.41249714C= , CM000663.1:g.41249714C= GRCh37
NC_000001.9:g.41022301C= NCBI36
NG_008139.1:g.5031C=
NG_008139.2:g.5031C=
NG_008139.3:g.5256C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.-52C= MANE Select ENSP00000262916.6:n.-52C=
ENST00000347132.9:c.-52C= ENSP00000262916.6:n.-52C=
NM_004700.3:c.-52C= NP_004691.2:n.-52C=
NM_172163.2:c.-52C= NP_751895.1:n.-52C=
NM_004700.4:c.-52C= MANE Select NP_004691.2:n.-52C=
NM_172163.3:c.-52C= NP_751895.1:n.-52C=