Canonical Allele Identifier: CA794472

Gene: KCNQ4

Linked Data

• dbSNP Id: rs772740345
• ExAC: 1:41250020 C / G
• gnomAD v2: 1-41250020-C-G
• gnomAD v3: 1-40784348-C-G
• gnomAD v4: 1-40784348-C-G
• MyVariant Identifiers: chr1:g.41250020C>G (hg19) ; chr1:g.40784348C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784348C>G , CM000663.2:g.40784348C>G	GRCh38
NC_000001.10:g.41250020C>G , CM000663.1:g.41250020C>G	GRCh37
NC_000001.9:g.41022607C>G	NCBI36
NG_008139.1:g.5337C>G
NG_008139.2:g.5337C>G
NG_008139.3:g.5562C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.255C>G MANE Select	ENSP00000262916.6:p.Asn85Lys
ENST00000347132.9:c.255C>G	ENSP00000262916.6:p.Asn85Lys
ENST00000509682.6:c.255C>G	ENSP00000423756.2:p.Asn85Lys
NM_004700.3:c.255C>G	NP_004691.2:p.Asn85Lys
NM_172163.2:c.255C>G	NP_751895.1:p.Asn85Lys
XM_011542417.1:c.255C>G	XP_011540719.1:p.Asn85Lys
XM_011542418.1:c.255C>G	XP_011540720.1:p.Asn85Lys
XM_011542419.1:c.255C>G	XP_011540721.1:p.Asn85Lys
XM_011542420.1:c.255C>G	XP_011540722.1:p.Asn85Lys
XR_946798.1:n.261C>G
XR_946799.1:n.261C>G
XR_946800.1:n.261C>G
NM_004700.4:c.255C>G MANE Select	NP_004691.2:p.Asn85Lys
NM_172163.3:c.255C>G	NP_751895.1:p.Asn85Lys