Canonical Allele Identifier: CA2337655767

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776497_43776498delinsAG , CM000681.2:g.43776497_43776498delinsAG	GRCh38
NC_000019.9:g.44280649_44280650delinsAG , CM000681.1:g.44280649_44280650delinsAG	GRCh37
NC_000019.8:g.48972489_48972490delinsAG	NCBI36
NG_052672.1:g.10642_10643delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+43_255+44delinsCT MANE Select	ENSP00000496939.1:n.255+43_255+44delinsCT
ENST00000262888.7:c.255+43_255+44delinsCT	ENSP00000262888.3:n.255+43_255+44delinsCT
ENST00000599107.1:n.286+43_286+44delinsCT
ENST00000599720.5:c.159+4205_159+4206delinsCT	ENSP00000472513.1:n.159+4205_159+4206delinsCT
ENST00000615047.4:c.70+43_70+44delinsCT	ENSP00000485014.1:n.70+43_70+44delinsCT
NM_002250.2:c.255+43_255+44delinsCT	NP_002241.1:n.255+43_255+44delinsCT
XM_005258882.2:c.160-1879_160-1878delinsCT	XP_005258939.1:n.160-1879_160-1878delinsCT
XM_005258883.2:c.70+43_70+44delinsCT	XP_005258940.1:n.70+43_70+44delinsCT
XM_011526938.1:c.255+43_255+44delinsCT	XP_011525240.1:n.255+43_255+44delinsCT
XR_935823.1:n.1533+43_1533+44delinsCT
XR_002958313.1:n.1533+43_1533+44delinsCT
NM_002250.3:c.255+43_255+44delinsCT MANE Select	NP_002241.1:n.255+43_255+44delinsCT