Canonical Allele Identifier: CA2337655698

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776348G= , CM000681.2:g.43776348G=	GRCh38
NC_000019.9:g.44280500G= , CM000681.1:g.44280500G=	GRCh37
NC_000019.8:g.48972340G=	NCBI36
NG_052672.1:g.10792C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000648319.1:c.255+193C= MANE Select	ENSP00000496939.1:n.255+193C=
ENST00000262888.7:c.255+193C=	ENSP00000262888.3:n.255+193C=
ENST00000599107.1:n.286+193C=
ENST00000599720.5:c.160-4245C=	ENSP00000472513.1:n.160-4245C=
ENST00000615047.4:c.70+193C=	ENSP00000485014.1:n.70+193C=
NM_002250.2:c.255+193C=	NP_002241.1:n.255+193C=
XM_005258882.2:c.160-1729C=	XP_005258939.1:n.160-1729C=
XM_005258883.2:c.70+193C=	XP_005258940.1:n.70+193C=
XM_011526938.1:c.255+193C=	XP_011525240.1:n.255+193C=
XR_935823.1:n.1533+193C=
XR_002958313.1:n.1533+193C=
NM_002250.3:c.255+193C= MANE Select	NP_002241.1:n.255+193C=