Canonical Allele Identifier: CA2337652648

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769813G= , CM000681.2:g.43769813G=	GRCh38
NC_000019.9:g.44273965G= , CM000681.1:g.44273965G=	GRCh37
NC_000019.8:g.48965805G=	NCBI36
NG_052672.1:g.17327C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000601549.2:n.458C=
ENST00000648053.1:n.268C=
ENST00000648319.1:c.836C= MANE Select	ENSP00000496939.1:p.Ala279=
ENST00000262888.7:c.836C=	ENSP00000262888.3:p.Ala279=
ENST00000598836.1:c.15C=
ENST00000599720.5:c.*106C=	ENSP00000472513.1:n.*106C=
ENST00000600408.1:c.125C=	ENSP00000472510.1:p.Ala42=
ENST00000601549.1:n.145C=
ENST00000615047.4:c.440C=	ENSP00000485014.1:p.Ala147=
NM_002250.2:c.836C=	NP_002241.1:p.Ala279=
XM_005258882.2:c.740C=	XP_005258939.1:p.Ala247=
XM_005258883.2:c.647C=	XP_005258940.1:p.Ala216=
XR_935823.1:n.2082C=
XR_002958313.1:n.2228C=
NM_002250.3:c.836C= MANE Select	NP_002241.1:p.Ala279=