Canonical Allele Identifier: CA996174934

Gene: KCNN4

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776158del , CM000681.2:g.43776158del	GRCh38
NC_000019.9:g.44280310del , CM000681.1:g.44280310del	GRCh37
NC_000019.8:g.48972150del	NCBI36
NG_052672.1:g.10983del

Transcript Alleles

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