Canonical Allele Identifier: CA2585562079
Gene: KCNN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43769870_43769871insCTGTGGGCACA , CM000681.2:g.43769870_43769871insCTGTGGGCACA GRCh38
NC_000019.9:g.44274022_44274023insCTGTGGGCACA , CM000681.1:g.44274022_44274023insCTGTGGGCACA GRCh37
NC_000019.8:g.48965862_48965863insCTGTGGGCACA NCBI36
NG_052672.1:g.17269_17270insTGTGCCCACAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000601549.2:n.442-42_442-41insTGTGCCCACAG
ENST00000648053.1:n.252-42_252-41insTGTGCCCACAG
ENST00000648319.1:c.820-42_820-41insTGTGCCCACAG MANE Select ENSP00000496939.1:n.820-42_820-41insTGTGCCCACAG
ENST00000262888.7:c.820-42_820-41insTGTGCCCACAG ENSP00000262888.3:n.820-42_820-41insTGTGCCCACAG
ENST00000599720.5:c.*90-42_*90-41insTGTGCCCACAG ENSP00000472513.1:n.*90-42_*90-41insTGTGCCCACAG
ENST00000600408.1:c.109-42_109-41insTGTGCCCACAG ENSP00000472510.1:n.109-42_109-41insTGTGCCCACAG
ENST00000601549.1:n.129-42_129-41insTGTGCCCACAG
ENST00000615047.4:c.424-42_424-41insTGTGCCCACAG ENSP00000485014.1:n.424-42_424-41insTGTGCCCACAG
NM_002250.2:c.820-42_820-41insTGTGCCCACAG NP_002241.1:n.820-42_820-41insTGTGCCCACAG
XM_005258882.2:c.724-42_724-41insTGTGCCCACAG XP_005258939.1:n.724-42_724-41insTGTGCCCACAG
XM_005258883.2:c.631-42_631-41insTGTGCCCACAG XP_005258940.1:n.631-42_631-41insTGTGCCCACAG
XR_935823.1:n.2066-42_2066-41insTGTGCCCACAG
XR_002958313.1:n.2212-42_2212-41insTGTGCCCACAG
NM_002250.3:c.820-42_820-41insTGTGCCCACAG MANE Select NP_002241.1:n.820-42_820-41insTGTGCCCACAG