Canonical Allele Identifier: CA1164531013

Gene: KCNQ4

Linked Data

• dbSNP Id: rs1647179100
• gnomAD v4: 1-40784013-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784013G>T , CM000663.2:g.40784013G>T	GRCh38
NC_000001.10:g.41249685G>T , CM000663.1:g.41249685G>T	GRCh37
NC_000001.9:g.41022272G>T	NCBI36
NG_008139.1:g.5002G>T
NG_008139.2:g.5002G>T
NG_008139.3:g.5227G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.-81G>T MANE Select	ENSP00000262916.6:n.-81G>T
ENST00000347132.9:c.-81G>T	ENSP00000262916.6:n.-81G>T
NM_004700.3:c.-81G>T	NP_004691.2:n.-81G>T
NM_172163.2:c.-81G>T	NP_751895.1:n.-81G>T
NM_004700.4:c.-81G>T MANE Select	NP_004691.2:n.-81G>T
NM_172163.3:c.-81G>T	NP_751895.1:n.-81G>T