Canonical Allele Identifier: CA2337652650

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769826C= , CM000681.2:g.43769826C=	GRCh38
NC_000019.9:g.44273978C= , CM000681.1:g.44273978C=	GRCh37
NC_000019.8:g.48965818C=	NCBI36
NG_052672.1:g.17314G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.445G=
ENST00000648053.1:n.255G=
ENST00000648319.1:c.823G= MANE Select	ENSP00000496939.1:p.Val275=
ENST00000262888.7:c.823G=	ENSP00000262888.3:p.Val275=
ENST00000598836.1:c.2G=
ENST00000599720.5:c.*93G=	ENSP00000472513.1:n.*93G=
ENST00000600408.1:c.112G=	ENSP00000472510.1:p.Val38=
ENST00000601549.1:n.132G=
ENST00000615047.4:c.427G=	ENSP00000485014.1:p.Val143=
NM_002250.2:c.823G=	NP_002241.1:p.Val275=
XM_005258882.2:c.727G=	XP_005258939.1:p.Val243=
XM_005258883.2:c.634G=	XP_005258940.1:p.Val212=
XR_935823.1:n.2069G=
XR_002958313.1:n.2215G=
NM_002250.3:c.823G= MANE Select	NP_002241.1:p.Val275=