Canonical Allele Identifier: CA996176077

Gene: KCNN4

Linked Data

• dbSNP Id: rs670950
• gnomAD v3: 19-43777410-T-A
• gnomAD v4: 19-43777410-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43777410T>A , CM000681.2:g.43777410T>A	GRCh38
NC_000019.9:g.44281562T>A , CM000681.1:g.44281562T>A	GRCh37
NC_000019.8:g.48973402T>A	NCBI36
NG_052672.1:g.9730A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.160-774A>T MANE Select	ENSP00000496939.1:n.160-774A>T
ENST00000262888.7:c.160-774A>T	ENSP00000262888.3:n.160-774A>T
ENST00000599720.5:c.159+3293A>T	ENSP00000472513.1:n.159+3293A>T
ENST00000615047.4:c.-26-774A>T	ENSP00000485014.1:n.-26-774A>T
NM_002250.2:c.160-774A>T	NP_002241.1:n.160-774A>T
XM_005258882.2:c.160-2791A>T	XP_005258939.1:n.160-2791A>T
XM_005258883.2:c.-26-774A>T	XP_005258940.1:n.-26-774A>T
XM_011526938.1:c.160-774A>T	XP_011525240.1:n.160-774A>T
XR_935823.1:n.1438-774A>T
XR_002958313.1:n.1438-774A>T
NM_002250.3:c.160-774A>T MANE Select	NP_002241.1:n.160-774A>T