Canonical Allele Identifier: CA2585562125

Gene: KCNN4

Linked Data

• gnomAD v4: 19-43769905-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769905C>A , CM000681.2:g.43769905C>A	GRCh38
NC_000019.9:g.44274057C>A , CM000681.1:g.44274057C>A	GRCh37
NC_000019.8:g.48965897C>A	NCBI36
NG_052672.1:g.17235G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.442-76G>T
ENST00000648053.1:n.252-76G>T
ENST00000648319.1:c.820-76G>T MANE Select	ENSP00000496939.1:n.820-76G>T
ENST00000262888.7:c.820-76G>T	ENSP00000262888.3:n.820-76G>T
ENST00000599720.5:c.*90-76G>T	ENSP00000472513.1:n.*90-76G>T
ENST00000600408.1:c.109-76G>T	ENSP00000472510.1:n.109-76G>T
ENST00000601549.1:n.129-76G>T
ENST00000615047.4:c.424-76G>T	ENSP00000485014.1:n.424-76G>T
NM_002250.2:c.820-76G>T	NP_002241.1:n.820-76G>T
XM_005258882.2:c.724-76G>T	XP_005258939.1:n.724-76G>T
XM_005258883.2:c.631-76G>T	XP_005258940.1:n.631-76G>T
XR_935823.1:n.2066-76G>T
XR_002958313.1:n.2212-76G>T
NM_002250.3:c.820-76G>T MANE Select	NP_002241.1:n.820-76G>T