Canonical Allele Identifier: CA2337652623

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769757C= , CM000681.2:g.43769757C=	GRCh38
NC_000019.9:g.44273909C= , CM000681.1:g.44273909C=	GRCh37
NC_000019.8:g.48965749C=	NCBI36
NG_052672.1:g.17383G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.514G=
ENST00000648053.1:n.324G=
ENST00000648319.1:c.892G= MANE Select	ENSP00000496939.1:p.Val298=
ENST00000262888.7:c.892G=	ENSP00000262888.3:p.Val298=
ENST00000598836.1:c.71G=
ENST00000599720.5:c.*162G=	ENSP00000472513.1:n.*162G=
ENST00000600408.1:c.181G=	ENSP00000472510.1:p.Val61=
ENST00000601549.1:n.201G=
ENST00000615047.4:c.496G=	ENSP00000485014.1:p.Val166=
NM_002250.2:c.892G=	NP_002241.1:p.Val298=
XM_005258882.2:c.796G=	XP_005258939.1:p.Val266=
XM_005258883.2:c.703G=	XP_005258940.1:p.Val235=
XR_935823.1:n.2138G=
XR_002958313.1:n.2284G=
NM_002250.3:c.892G= MANE Select	NP_002241.1:p.Val298=