Canonical Allele Identifier: CA2337652633

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769785C= , CM000681.2:g.43769785C=	GRCh38
NC_000019.9:g.44273937C= , CM000681.1:g.44273937C=	GRCh37
NC_000019.8:g.48965777C=	NCBI36
NG_052672.1:g.17355G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.486G=
ENST00000648053.1:n.296G=
ENST00000648319.1:c.864G= MANE Select	ENSP00000496939.1:p.Lys288=
ENST00000262888.7:c.864G=	ENSP00000262888.3:p.Lys288=
ENST00000598836.1:c.43G=
ENST00000599720.5:c.*134G=	ENSP00000472513.1:n.*134G=
ENST00000600408.1:c.153G=	ENSP00000472510.1:p.Lys51=
ENST00000601549.1:n.173G=
ENST00000615047.4:c.468G=	ENSP00000485014.1:p.Lys156=
NM_002250.2:c.864G=	NP_002241.1:p.Lys288=
XM_005258882.2:c.768G=	XP_005258939.1:p.Lys256=
XM_005258883.2:c.675G=	XP_005258940.1:p.Lys225=
XR_935823.1:n.2110G=
XR_002958313.1:n.2256G=
NM_002250.3:c.864G= MANE Select	NP_002241.1:p.Lys288=