Canonical Allele Identifier: CA2337652641

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769800G= , CM000681.2:g.43769800G=	GRCh38
NC_000019.9:g.44273952G= , CM000681.1:g.44273952G=	GRCh37
NC_000019.8:g.48965792G=	NCBI36
NG_052672.1:g.17340C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.471C=
ENST00000648053.1:n.281C=
ENST00000648319.1:c.849C= MANE Select	ENSP00000496939.1:p.Ala283=
ENST00000262888.7:c.849C=	ENSP00000262888.3:p.Ala283=
ENST00000598836.1:c.28C=
ENST00000599720.5:c.*119C=	ENSP00000472513.1:n.*119C=
ENST00000600408.1:c.138C=	ENSP00000472510.1:p.Ala46=
ENST00000601549.1:n.158C=
ENST00000615047.4:c.453C=	ENSP00000485014.1:p.Ala151=
NM_002250.2:c.849C=	NP_002241.1:p.Ala283=
XM_005258882.2:c.753C=	XP_005258939.1:p.Ala251=
XM_005258883.2:c.660C=	XP_005258940.1:p.Ala220=
XR_935823.1:n.2095C=
XR_002958313.1:n.2241C=
NM_002250.3:c.849C= MANE Select	NP_002241.1:p.Ala283=