Canonical Allele Identifier: CA2337655665

Gene: KCNN4

Linked Data

• dbSNP Id: rs1599679199

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776295A>C , CM000681.2:g.43776295A>C	GRCh38
NC_000019.9:g.44280447A>C , CM000681.1:g.44280447A>C	GRCh37
NC_000019.8:g.48972287A>C	NCBI36
NG_052672.1:g.10845T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+246T>G MANE Select	ENSP00000496939.1:n.255+246T>G
ENST00000262888.7:c.255+246T>G	ENSP00000262888.3:n.255+246T>G
ENST00000599107.1:n.286+246T>G
ENST00000599720.5:c.160-4192T>G	ENSP00000472513.1:n.160-4192T>G
ENST00000615047.4:c.70+246T>G	ENSP00000485014.1:n.70+246T>G
NM_002250.2:c.255+246T>G	NP_002241.1:n.255+246T>G
XM_005258882.2:c.160-1676T>G	XP_005258939.1:n.160-1676T>G
XM_005258883.2:c.70+246T>G	XP_005258940.1:n.70+246T>G
XM_011526938.1:c.255+246T>G	XP_011525240.1:n.255+246T>G
XR_935823.1:n.1533+246T>G
XR_002958313.1:n.1533+246T>G
NM_002250.3:c.255+246T>G MANE Select	NP_002241.1:n.255+246T>G