Canonical Allele Identifier: CA2814503211

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43775934_43775935insAT , CM000681.2:g.43775934_43775935insAT	GRCh38
NC_000019.9:g.44280086_44280087insAT , CM000681.1:g.44280086_44280087insAT	GRCh37
NC_000019.8:g.48971926_48971927insAT	NCBI36
NG_052672.1:g.11205_11206insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+606_255+607insAT MANE Select	ENSP00000496939.1:n.255+606_255+607insAT
ENST00000262888.7:c.255+606_255+607insAT	ENSP00000262888.3:n.255+606_255+607insAT
ENST00000599107.1:n.286+606_286+607insAT
ENST00000599720.5:c.160-3832_160-3831insAT	ENSP00000472513.1:n.160-3832_160-3831insAT
ENST00000615047.4:c.70+606_70+607insAT	ENSP00000485014.1:n.70+606_70+607insAT
NM_002250.2:c.255+606_255+607insAT	NP_002241.1:n.255+606_255+607insAT
XM_005258882.2:c.160-1316_160-1315insAT	XP_005258939.1:n.160-1316_160-1315insAT
XM_005258883.2:c.70+606_70+607insAT	XP_005258940.1:n.70+606_70+607insAT
XM_011526938.1:c.255+606_255+607insAT	XP_011525240.1:n.255+606_255+607insAT
XR_935823.1:n.1533+606_1533+607insAT
XR_002958313.1:n.1533+606_1533+607insAT
NM_002250.3:c.255+606_255+607insAT MANE Select	NP_002241.1:n.255+606_255+607insAT