Canonical Allele Identifier: CA2337652688

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769898C= , CM000681.2:g.43769898C=	GRCh38
NC_000019.9:g.44274050C= , CM000681.1:g.44274050C=	GRCh37
NC_000019.8:g.48965890C=	NCBI36
NG_052672.1:g.17242G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.442-69G=
ENST00000648053.1:n.252-69G=
ENST00000648319.1:c.820-69G= MANE Select	ENSP00000496939.1:n.820-69G=
ENST00000262888.7:c.820-69G=	ENSP00000262888.3:n.820-69G=
ENST00000599720.5:c.*90-69G=	ENSP00000472513.1:n.*90-69G=
ENST00000600408.1:c.109-69G=	ENSP00000472510.1:n.109-69G=
ENST00000601549.1:n.129-69G=
ENST00000615047.4:c.424-69G=	ENSP00000485014.1:n.424-69G=
NM_002250.2:c.820-69G=	NP_002241.1:n.820-69G=
XM_005258882.2:c.724-69G=	XP_005258939.1:n.724-69G=
XM_005258883.2:c.631-69G=	XP_005258940.1:n.631-69G=
XR_935823.1:n.2066-69G=
XR_002958313.1:n.2212-69G=
NM_002250.3:c.820-69G= MANE Select	NP_002241.1:n.820-69G=