Canonical Allele Identifier: CA2585562099

Gene: KCNN4

Linked Data

• gnomAD v4: 19-43769887-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769887C>G , CM000681.2:g.43769887C>G	GRCh38
NC_000019.9:g.44274039C>G , CM000681.1:g.44274039C>G	GRCh37
NC_000019.8:g.48965879C>G	NCBI36
NG_052672.1:g.17253G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.442-58G>C
ENST00000648053.1:n.252-58G>C
ENST00000648319.1:c.820-58G>C MANE Select	ENSP00000496939.1:n.820-58G>C
ENST00000262888.7:c.820-58G>C	ENSP00000262888.3:n.820-58G>C
ENST00000599720.5:c.*90-58G>C	ENSP00000472513.1:n.*90-58G>C
ENST00000600408.1:c.109-58G>C	ENSP00000472510.1:n.109-58G>C
ENST00000601549.1:n.129-58G>C
ENST00000615047.4:c.424-58G>C	ENSP00000485014.1:n.424-58G>C
NM_002250.2:c.820-58G>C	NP_002241.1:n.820-58G>C
XM_005258882.2:c.724-58G>C	XP_005258939.1:n.724-58G>C
XM_005258883.2:c.631-58G>C	XP_005258940.1:n.631-58G>C
XR_935823.1:n.2066-58G>C
XR_002958313.1:n.2212-58G>C
NM_002250.3:c.820-58G>C MANE Select	NP_002241.1:n.820-58G>C