Canonical Allele Identifier: CA1164530996
Gene: KCNQ4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40783975G= , CM000663.2:g.40783975G= GRCh38
NC_000001.10:g.41249647G= , CM000663.1:g.41249647G= GRCh37
NC_000001.9:g.41022234G= NCBI36
NG_008139.1:g.4964G=
NG_008139.2:g.4964G=
NG_008139.3:g.5189G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.-119G= MANE Select ENSP00000262916.6:n.-119G=
NM_004700.4:c.-119G= MANE Select NP_004691.2:n.-119G=
NM_172163.3:c.-119G= NP_751895.1:n.-119G=