Canonical Allele Identifier: CA2337656286

Gene: KCNN4

Linked Data

• dbSNP Id: rs670950

Genomic Alleles

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

Transcript Alleles

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