Canonical Allele Identifier: CA2576806576

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776463_43776468del , CM000681.2:g.43776463_43776468del	GRCh38
NC_000019.9:g.44280615_44280620del , CM000681.1:g.44280615_44280620del	GRCh37
NC_000019.8:g.48972455_48972460del	NCBI36
NG_052672.1:g.10681_10686del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+82_255+87del MANE Select	ENSP00000496939.1:n.255+82_255+87del
ENST00000262888.7:c.255+82_255+87del	ENSP00000262888.3:n.255+82_255+87del
ENST00000599107.1:n.286+82_286+87del
ENST00000599720.5:c.159+4244_159+4249del	ENSP00000472513.1:n.159+4244_159+4249del
ENST00000615047.4:c.70+82_70+87del	ENSP00000485014.1:n.70+82_70+87del
NM_002250.2:c.255+82_255+87del	NP_002241.1:n.255+82_255+87del
XM_005258882.2:c.160-1840_160-1835del	XP_005258939.1:n.160-1840_160-1835del
XM_005258883.2:c.70+82_70+87del	XP_005258940.1:n.70+82_70+87del
XM_011526938.1:c.255+82_255+87del	XP_011525240.1:n.255+82_255+87del
XR_935823.1:n.1533+82_1533+87del
XR_002958313.1:n.1533+82_1533+87del
NM_002250.3:c.255+82_255+87del MANE Select	NP_002241.1:n.255+82_255+87del