Canonical Allele Identifier: CA2337655749

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776466_43776467delinsAG , CM000681.2:g.43776466_43776467delinsAG	GRCh38
NC_000019.9:g.44280618_44280619delinsAG , CM000681.1:g.44280618_44280619delinsAG	GRCh37
NC_000019.8:g.48972458_48972459delinsAG	NCBI36
NG_052672.1:g.10673_10674delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+74_255+75delinsCT MANE Select	ENSP00000496939.1:n.255+74_255+75delinsCT
ENST00000262888.7:c.255+74_255+75delinsCT	ENSP00000262888.3:n.255+74_255+75delinsCT
ENST00000599107.1:n.286+74_286+75delinsCT
ENST00000599720.5:c.159+4236_159+4237delinsCT	ENSP00000472513.1:n.159+4236_159+4237delinsCT
ENST00000615047.4:c.70+74_70+75delinsCT	ENSP00000485014.1:n.70+74_70+75delinsCT
NM_002250.2:c.255+74_255+75delinsCT	NP_002241.1:n.255+74_255+75delinsCT
XM_005258882.2:c.160-1848_160-1847delinsCT	XP_005258939.1:n.160-1848_160-1847delinsCT
XM_005258883.2:c.70+74_70+75delinsCT	XP_005258940.1:n.70+74_70+75delinsCT
XM_011526938.1:c.255+74_255+75delinsCT	XP_011525240.1:n.255+74_255+75delinsCT
XR_935823.1:n.1533+74_1533+75delinsCT
XR_002958313.1:n.1533+74_1533+75delinsCT
NM_002250.3:c.255+74_255+75delinsCT MANE Select	NP_002241.1:n.255+74_255+75delinsCT