Canonical Allele Identifier: CA339895892

Gene: KCNQ4

Linked Data

• MyVariant Identifiers: chr1:g.41285578A>C (hg19) ; chr1:g.40819906A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819906A>C , CM000663.2:g.40819906A>C	GRCh38
NC_000001.10:g.41285578A>C , CM000663.1:g.41285578A>C	GRCh37
NC_000001.9:g.41058165A>C	NCBI36
NG_008139.1:g.40895A>C
NG_008139.2:g.40895A>C
NG_008139.3:g.41120A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000347132.10:c.866A>C MANE Select	ENSP00000262916.6:p.Lys289Thr
ENST00000347132.9:c.866A>C	ENSP00000262916.6:p.Lys289Thr
ENST00000443478.3:c.552A>C
ENST00000506017.1:n.185A>C
ENST00000509682.6:c.866A>C	ENSP00000423756.2:p.Lys289Thr
NM_004700.3:c.866A>C	NP_004691.2:p.Lys289Thr
NM_172163.2:c.866A>C	NP_751895.1:p.Lys289Thr
XM_011542417.1:c.866A>C	XP_011540719.1:p.Lys289Thr
XM_011542418.1:c.866A>C	XP_011540720.1:p.Lys289Thr
XM_011542419.1:c.866A>C	XP_011540721.1:p.Lys289Thr
XM_011542420.1:c.866A>C	XP_011540722.1:p.Lys289Thr
XR_946798.1:n.872A>C
XR_946799.1:n.872A>C
XR_946800.1:n.872A>C
XM_017002792.1:c.-152A>C	XP_016858281.1:n.-152A>C
NM_004700.4:c.866A>C MANE Select	NP_004691.2:p.Lys289Thr
NM_172163.3:c.866A>C	NP_751895.1:p.Lys289Thr