Canonical Allele Identifier: CA2585562080

Gene: KCNN4

Linked Data

• gnomAD v4: 19-43769871-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769871G>T , CM000681.2:g.43769871G>T	GRCh38
NC_000019.9:g.44274023G>T , CM000681.1:g.44274023G>T	GRCh37
NC_000019.8:g.48965863G>T	NCBI36
NG_052672.1:g.17269C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.442-42C>A
ENST00000648053.1:n.252-42C>A
ENST00000648319.1:c.820-42C>A MANE Select	ENSP00000496939.1:n.820-42C>A
ENST00000262888.7:c.820-42C>A	ENSP00000262888.3:n.820-42C>A
ENST00000599720.5:c.*90-42C>A	ENSP00000472513.1:n.*90-42C>A
ENST00000600408.1:c.109-42C>A	ENSP00000472510.1:n.109-42C>A
ENST00000601549.1:n.129-42C>A
ENST00000615047.4:c.424-42C>A	ENSP00000485014.1:n.424-42C>A
NM_002250.2:c.820-42C>A	NP_002241.1:n.820-42C>A
XM_005258882.2:c.724-42C>A	XP_005258939.1:n.724-42C>A
XM_005258883.2:c.631-42C>A	XP_005258940.1:n.631-42C>A
XR_935823.1:n.2066-42C>A
XR_002958313.1:n.2212-42C>A
NM_002250.3:c.820-42C>A MANE Select	NP_002241.1:n.820-42C>A