Canonical Allele Identifier: CA657379485

Gene: KCNN4

Linked Data

• COSMIC: COSN1216298

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776293G>T , CM000681.2:g.43776293G>T	GRCh38
NC_000019.9:g.44280445G>T , CM000681.1:g.44280445G>T	GRCh37
NC_000019.8:g.48972285G>T	NCBI36
NG_052672.1:g.10847C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+248C>A MANE Select	ENSP00000496939.1:n.255+248C>A
ENST00000262888.7:c.255+248C>A	ENSP00000262888.3:n.255+248C>A
ENST00000599107.1:n.286+248C>A
ENST00000599720.5:c.160-4190C>A	ENSP00000472513.1:n.160-4190C>A
ENST00000615047.4:c.70+248C>A	ENSP00000485014.1:n.70+248C>A
NM_002250.2:c.255+248C>A	NP_002241.1:n.255+248C>A
XM_005258882.2:c.160-1674C>A	XP_005258939.1:n.160-1674C>A
XM_005258883.2:c.70+248C>A	XP_005258940.1:n.70+248C>A
XM_011526938.1:c.255+248C>A	XP_011525240.1:n.255+248C>A
XR_935823.1:n.1533+248C>A
XR_002958313.1:n.1533+248C>A
NM_002250.3:c.255+248C>A MANE Select	NP_002241.1:n.255+248C>A