Canonical Allele Identifier: CA2576806494

Gene: KCNN4

Linked Data

• gnomAD v4: 19-43769882-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769882T>C , CM000681.2:g.43769882T>C	GRCh38
NC_000019.9:g.44274034T>C , CM000681.1:g.44274034T>C	GRCh37
NC_000019.8:g.48965874T>C	NCBI36
NG_052672.1:g.17258A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.442-53A>G
ENST00000648053.1:n.252-53A>G
ENST00000648319.1:c.820-53A>G MANE Select	ENSP00000496939.1:n.820-53A>G
ENST00000262888.7:c.820-53A>G	ENSP00000262888.3:n.820-53A>G
ENST00000599720.5:c.*90-53A>G	ENSP00000472513.1:n.*90-53A>G
ENST00000600408.1:c.109-53A>G	ENSP00000472510.1:n.109-53A>G
ENST00000601549.1:n.129-53A>G
ENST00000615047.4:c.424-53A>G	ENSP00000485014.1:n.424-53A>G
NM_002250.2:c.820-53A>G	NP_002241.1:n.820-53A>G
XM_005258882.2:c.724-53A>G	XP_005258939.1:n.724-53A>G
XM_005258883.2:c.631-53A>G	XP_005258940.1:n.631-53A>G
XR_935823.1:n.2066-53A>G
XR_002958313.1:n.2212-53A>G
NM_002250.3:c.820-53A>G MANE Select	NP_002241.1:n.820-53A>G