Canonical Allele Identifier: CA996174921

Gene: KCNN4

Linked Data

• gnomAD v3: 19-43776155-A-AGG
• gnomAD v4: 19-43776155-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776155_43776156insGG , CM000681.2:g.43776155_43776156insGG	GRCh38
NC_000019.9:g.44280307_44280308insGG , CM000681.1:g.44280307_44280308insGG	GRCh37
NC_000019.8:g.48972147_48972148insGG	NCBI36
NG_052672.1:g.10984_10985insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+385_255+386insCC MANE Select	ENSP00000496939.1:n.255+385_255+386insCC
ENST00000262888.7:c.255+385_255+386insCC	ENSP00000262888.3:n.255+385_255+386insCC
ENST00000599107.1:n.286+385_286+386insCC
ENST00000599720.5:c.160-4053_160-4052insCC	ENSP00000472513.1:n.160-4053_160-4052insCC
ENST00000615047.4:c.70+385_70+386insCC	ENSP00000485014.1:n.70+385_70+386insCC
NM_002250.2:c.255+385_255+386insCC	NP_002241.1:n.255+385_255+386insCC
XM_005258882.2:c.160-1537_160-1536insCC	XP_005258939.1:n.160-1537_160-1536insCC
XM_005258883.2:c.70+385_70+386insCC	XP_005258940.1:n.70+385_70+386insCC
XM_011526938.1:c.255+385_255+386insCC	XP_011525240.1:n.255+385_255+386insCC
XR_935823.1:n.1533+385_1533+386insCC
XR_002958313.1:n.1533+385_1533+386insCC
NM_002250.3:c.255+385_255+386insCC MANE Select	NP_002241.1:n.255+385_255+386insCC