Canonical Allele Identifier: CA2337652682

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43769883_43769884delinsGA , CM000681.2:g.43769883_43769884delinsGA	GRCh38
NC_000019.9:g.44274035_44274036delinsGA , CM000681.1:g.44274035_44274036delinsGA	GRCh37
NC_000019.8:g.48965875_48965876delinsGA	NCBI36
NG_052672.1:g.17256_17257delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000601549.2:n.442-55_442-54delinsTC
ENST00000648053.1:n.252-55_252-54delinsTC
ENST00000648319.1:c.820-55_820-54delinsTC MANE Select	ENSP00000496939.1:n.820-55_820-54delinsTC
ENST00000262888.7:c.820-55_820-54delinsTC	ENSP00000262888.3:n.820-55_820-54delinsTC
ENST00000599720.5:c.*90-55_*90-54delinsTC	ENSP00000472513.1:n.*90-55_*90-54delinsTC
ENST00000600408.1:c.109-55_109-54delinsTC	ENSP00000472510.1:n.109-55_109-54delinsTC
ENST00000601549.1:n.129-55_129-54delinsTC
ENST00000615047.4:c.424-55_424-54delinsTC	ENSP00000485014.1:n.424-55_424-54delinsTC
NM_002250.2:c.820-55_820-54delinsTC	NP_002241.1:n.820-55_820-54delinsTC
XM_005258882.2:c.724-55_724-54delinsTC	XP_005258939.1:n.724-55_724-54delinsTC
XM_005258883.2:c.631-55_631-54delinsTC	XP_005258940.1:n.631-55_631-54delinsTC
XR_935823.1:n.2066-55_2066-54delinsTC
XR_002958313.1:n.2212-55_2212-54delinsTC
NM_002250.3:c.820-55_820-54delinsTC MANE Select	NP_002241.1:n.820-55_820-54delinsTC