Canonical Allele Identifier: CA2337652616

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769731C= , CM000681.2:g.43769731C=	GRCh38
NC_000019.9:g.44273883C= , CM000681.1:g.44273883C=	GRCh37
NC_000019.8:g.48965723C=	NCBI36
NG_052672.1:g.17409G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.540G=
ENST00000648053.1:n.350G=
ENST00000648319.1:c.918G= MANE Select	ENSP00000496939.1:p.Gln306=
ENST00000262888.7:c.918G=	ENSP00000262888.3:p.Gln306=
ENST00000598836.1:c.97G=
ENST00000599720.5:c.*188G=	ENSP00000472513.1:n.*188G=
ENST00000600408.1:c.207G=	ENSP00000472510.1:p.Gln69=
ENST00000601549.1:n.227G=
ENST00000615047.4:c.522G=	ENSP00000485014.1:p.Gln174=
NM_002250.2:c.918G=	NP_002241.1:p.Gln306=
XM_005258882.2:c.822G=	XP_005258939.1:p.Gln274=
XM_005258883.2:c.729G=	XP_005258940.1:p.Gln243=
XR_935823.1:n.2164G=
XR_002958313.1:n.2310G=
NM_002250.3:c.918G= MANE Select	NP_002241.1:p.Gln306=