Canonical Allele Identifier: CA2645130556
Gene: KCNQ4 HGNC NCBI

Linked Data

gnomAD v4: 1-40784016-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40784016A>T , CM000663.2:g.40784016A>T GRCh38
NC_000001.10:g.41249688A>T , CM000663.1:g.41249688A>T GRCh37
NC_000001.9:g.41022275A>T NCBI36
NG_008139.1:g.5005A>T
NG_008139.2:g.5005A>T
NG_008139.3:g.5230A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.-78A>T MANE Select ENSP00000262916.6:n.-78A>T
ENST00000347132.9:c.-78A>T ENSP00000262916.6:n.-78A>T
NM_004700.3:c.-78A>T NP_004691.2:n.-78A>T
NM_172163.2:c.-78A>T NP_751895.1:n.-78A>T
NM_004700.4:c.-78A>T MANE Select NP_004691.2:n.-78A>T
NM_172163.3:c.-78A>T NP_751895.1:n.-78A>T
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