Canonical Allele Identifier: CA2337655630

Gene: KCNN4

Linked Data

• dbSNP Id: rs1969799093
• gnomAD v3: 19-43776220-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776221dup , CM000681.2:g.43776221dup	GRCh38
NC_000019.9:g.44280373dup , CM000681.1:g.44280373dup	GRCh37
NC_000019.8:g.48972213dup	NCBI36
NG_052672.1:g.10919dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+320dup MANE Select	ENSP00000496939.1:n.255+320dup
ENST00000262888.7:c.255+320dup	ENSP00000262888.3:n.255+320dup
ENST00000599107.1:n.286+320dup
ENST00000599720.5:c.160-4118dup	ENSP00000472513.1:n.160-4118dup
ENST00000615047.4:c.70+320dup	ENSP00000485014.1:n.70+320dup
NM_002250.2:c.255+320dup	NP_002241.1:n.255+320dup
XM_005258882.2:c.160-1602dup	XP_005258939.1:n.160-1602dup
XM_005258883.2:c.70+320dup	XP_005258940.1:n.70+320dup
XM_011526938.1:c.255+320dup	XP_011525240.1:n.255+320dup
XR_935823.1:n.1533+320dup
XR_002958313.1:n.1533+320dup
NM_002250.3:c.255+320dup MANE Select	NP_002241.1:n.255+320dup