Canonical Allele Identifier: CA2645130831

Gene: KCNQ4

Linked Data

• gnomAD v4: 1-40784089-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784090del , CM000663.2:g.40784090del	GRCh38
NC_000001.10:g.41249762del , CM000663.1:g.41249762del	GRCh37
NC_000001.9:g.41022349del	NCBI36
NG_008139.1:g.5079del
NG_008139.2:g.5079del
NG_008139.3:g.5304del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.-4del MANE Select	ENSP00000262916.6:n.-4del
ENST00000347132.9:c.-4del	ENSP00000262916.6:n.-4del
NM_004700.3:c.-4del	NP_004691.2:n.-4del
NM_172163.2:c.-4del	NP_751895.1:n.-4del
XM_011542417.1:c.-4del	XP_011540719.1:n.-4del
XM_011542418.1:c.-4del	XP_011540720.1:n.-4del
XM_011542419.1:c.-4del	XP_011540721.1:n.-4del
XM_011542420.1:c.-4del	XP_011540722.1:n.-4del
XR_946798.1:n.3del
XR_946799.1:n.3del
XR_946800.1:n.3del
NM_004700.4:c.-4del MANE Select	NP_004691.2:n.-4del
NM_172163.3:c.-4del	NP_751895.1:n.-4del