Canonical Allele Identifier: CA2582182988

Gene: KCNN4

Linked Data

• gnomAD v3: 19-43776156-A-AAGGGGGGGGGGGGGG
• gnomAD v4: 19-43776156-A-AAGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776156_43776157insAGGGGGGGGGGGGGG , CM000681.2:g.43776156_43776157insAGGGGGGGGGGGGGG	GRCh38
NC_000019.9:g.44280308_44280309insAGGGGGGGGGGGGGG , CM000681.1:g.44280308_44280309insAGGGGGGGGGGGGGG	GRCh37
NC_000019.8:g.48972148_48972149insAGGGGGGGGGGGGGG	NCBI36
NG_052672.1:g.10983_10984insCCCCCCCCCCCCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+384_255+385insCCCCCCCCCCCCCCT MANE Select	ENSP00000496939.1:n.255+384_255+385insCCCCCCCCCCCCCCT
ENST00000262888.7:c.255+384_255+385insCCCCCCCCCCCCCCT	ENSP00000262888.3:n.255+384_255+385insCCCCCCCCCCCCCCT
ENST00000599107.1:n.286+384_286+385insCCCCCCCCCCCCCCT
ENST00000599720.5:c.160-4054_160-4053insCCCCCCCCCCCCCCT	ENSP00000472513.1:n.160-4054_160-4053insCCCCCCCCCCCCCCT
ENST00000615047.4:c.70+384_70+385insCCCCCCCCCCCCCCT	ENSP00000485014.1:n.70+384_70+385insCCCCCCCCCCCCCCT
NM_002250.2:c.255+384_255+385insCCCCCCCCCCCCCCT	NP_002241.1:n.255+384_255+385insCCCCCCCCCCCCCCT
XM_005258882.2:c.160-1538_160-1537insCCCCCCCCCCCCCCT	XP_005258939.1:n.160-1538_160-1537insCCCCCCCCCCCCCCT
XM_005258883.2:c.70+384_70+385insCCCCCCCCCCCCCCT	XP_005258940.1:n.70+384_70+385insCCCCCCCCCCCCCCT
XM_011526938.1:c.255+384_255+385insCCCCCCCCCCCCCCT	XP_011525240.1:n.255+384_255+385insCCCCCCCCCCCCCCT
XR_935823.1:n.1533+384_1533+385insCCCCCCCCCCCCCCT
XR_002958313.1:n.1533+384_1533+385insCCCCCCCCCCCCCCT
NM_002250.3:c.255+384_255+385insCCCCCCCCCCCCCCT MANE Select	NP_002241.1:n.255+384_255+385insCCCCCCCCCCCCCCT