Canonical Allele Identifier: CA920115256

Gene: KCNN4

Linked Data

• dbSNP Id: rs912661455

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43775978del , CM000681.2:g.43775978del	GRCh38
NC_000019.9:g.44280130del , CM000681.1:g.44280130del	GRCh37
NC_000019.8:g.48971970del	NCBI36
NG_052672.1:g.11168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+569del MANE Select	ENSP00000496939.1:n.255+569del
ENST00000262888.7:c.255+569del	ENSP00000262888.3:n.255+569del
ENST00000599107.1:n.286+569del
ENST00000599720.5:c.160-3869del	ENSP00000472513.1:n.160-3869del
ENST00000615047.4:c.70+569del	ENSP00000485014.1:n.70+569del
NM_002250.2:c.255+569del	NP_002241.1:n.255+569del
XM_005258882.2:c.160-1353del	XP_005258939.1:n.160-1353del
XM_005258883.2:c.70+569del	XP_005258940.1:n.70+569del
XM_011526938.1:c.255+569del	XP_011525240.1:n.255+569del
XR_935823.1:n.1533+569del
XR_002958313.1:n.1533+569del
NM_002250.3:c.255+569del MANE Select	NP_002241.1:n.255+569del