Canonical Allele Identifier: CA2337655452

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43775897_43775898delinsTG , CM000681.2:g.43775897_43775898delinsTG	GRCh38
NC_000019.9:g.44280049_44280050delinsTG , CM000681.1:g.44280049_44280050delinsTG	GRCh37
NC_000019.8:g.48971889_48971890delinsTG	NCBI36
NG_052672.1:g.11242_11243delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+643_255+644delinsCA MANE Select	ENSP00000496939.1:n.255+643_255+644delinsCA
ENST00000262888.7:c.255+643_255+644delinsCA	ENSP00000262888.3:n.255+643_255+644delinsCA
ENST00000599107.1:n.286+643_286+644delinsCA
ENST00000599720.5:c.160-3795_160-3794delinsCA	ENSP00000472513.1:n.160-3795_160-3794delinsCA
ENST00000615047.4:c.70+643_70+644delinsCA	ENSP00000485014.1:n.70+643_70+644delinsCA
NM_002250.2:c.255+643_255+644delinsCA	NP_002241.1:n.255+643_255+644delinsCA
XM_005258882.2:c.160-1279_160-1278delinsCA	XP_005258939.1:n.160-1279_160-1278delinsCA
XM_005258883.2:c.70+643_70+644delinsCA	XP_005258940.1:n.70+643_70+644delinsCA
XM_011526938.1:c.255+643_255+644delinsCA	XP_011525240.1:n.255+643_255+644delinsCA
XR_935823.1:n.1533+643_1533+644delinsCA
XR_002958313.1:n.1533+643_1533+644delinsCA
NM_002250.3:c.255+643_255+644delinsCA MANE Select	NP_002241.1:n.255+643_255+644delinsCA