Canonical Allele Identifier: CA2337652651

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769828C= , CM000681.2:g.43769828C=	GRCh38
NC_000019.9:g.44273980C= , CM000681.1:g.44273980C=	GRCh37
NC_000019.8:g.48965820C=	NCBI36
NG_052672.1:g.17312G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.443G=
ENST00000648053.1:n.253G=
ENST00000648319.1:c.821G= MANE Select	ENSP00000496939.1:p.Gly274=
ENST00000262888.7:c.821G=	ENSP00000262888.3:p.Gly274=
ENST00000599720.5:c.*91G=	ENSP00000472513.1:n.*91G=
ENST00000600408.1:c.110G=	ENSP00000472510.1:p.Gly37=
ENST00000601549.1:n.130G=
ENST00000615047.4:c.425G=	ENSP00000485014.1:p.Gly142=
NM_002250.2:c.821G=	NP_002241.1:p.Gly274=
XM_005258882.2:c.725G=	XP_005258939.1:p.Gly242=
XM_005258883.2:c.632G=	XP_005258940.1:p.Gly211=
XR_935823.1:n.2067G=
XR_002958313.1:n.2213G=
NM_002250.3:c.821G= MANE Select	NP_002241.1:p.Gly274=