Canonical Allele Identifier: CA2337655480

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43775971_43775972delinsCA , CM000681.2:g.43775971_43775972delinsCA	GRCh38
NC_000019.9:g.44280123_44280124delinsCA , CM000681.1:g.44280123_44280124delinsCA	GRCh37
NC_000019.8:g.48971963_48971964delinsCA	NCBI36
NG_052672.1:g.11168_11169delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+569_255+570delinsTG MANE Select	ENSP00000496939.1:n.255+569_255+570delinsTG
ENST00000262888.7:c.255+569_255+570delinsTG	ENSP00000262888.3:n.255+569_255+570delinsTG
ENST00000599107.1:n.286+569_286+570delinsTG
ENST00000599720.5:c.160-3869_160-3868delinsTG	ENSP00000472513.1:n.160-3869_160-3868delinsTG
ENST00000615047.4:c.70+569_70+570delinsTG	ENSP00000485014.1:n.70+569_70+570delinsTG
NM_002250.2:c.255+569_255+570delinsTG	NP_002241.1:n.255+569_255+570delinsTG
XM_005258882.2:c.160-1353_160-1352delinsTG	XP_005258939.1:n.160-1353_160-1352delinsTG
XM_005258883.2:c.70+569_70+570delinsTG	XP_005258940.1:n.70+569_70+570delinsTG
XM_011526938.1:c.255+569_255+570delinsTG	XP_011525240.1:n.255+569_255+570delinsTG
XR_935823.1:n.1533+569_1533+570delinsTG
XR_002958313.1:n.1533+569_1533+570delinsTG
NM_002250.3:c.255+569_255+570delinsTG MANE Select	NP_002241.1:n.255+569_255+570delinsTG