Canonical Allele Identifier: CA1164530978
Gene: KCNQ4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40783948C= , CM000663.2:g.40783948C= GRCh38
NC_000001.10:g.41249620C= , CM000663.1:g.41249620C= GRCh37
NC_000001.9:g.41022207C= NCBI36
NG_008139.1:g.4937C=
NG_008139.2:g.4937C=
NG_008139.3:g.5162C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.-146C= MANE Select ENSP00000262916.6:n.-146C=
NM_004700.4:c.-146C= MANE Select NP_004691.2:n.-146C=
NM_172163.3:c.-146C= NP_751895.1:n.-146C=
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