Canonical Allele Identifier: CA2830926160

Gene: KCNN4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776121_43776122del , CM000681.2:g.43776121_43776122del	GRCh38
NC_000019.9:g.44280273_44280274del , CM000681.1:g.44280273_44280274del	GRCh37
NC_000019.8:g.48972113_48972114del	NCBI36
NG_052672.1:g.11018_11019del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+419_255+420del MANE Select	ENSP00000496939.1:n.255+419_255+420del
ENST00000262888.7:c.255+419_255+420del	ENSP00000262888.3:n.255+419_255+420del
ENST00000599107.1:n.286+419_286+420del
ENST00000599720.5:c.160-4019_160-4018del	ENSP00000472513.1:n.160-4019_160-4018del
ENST00000615047.4:c.70+419_70+420del	ENSP00000485014.1:n.70+419_70+420del
NM_002250.2:c.255+419_255+420del	NP_002241.1:n.255+419_255+420del
XM_005258882.2:c.160-1503_160-1502del	XP_005258939.1:n.160-1503_160-1502del
XM_005258883.2:c.70+419_70+420del	XP_005258940.1:n.70+419_70+420del
XM_011526938.1:c.255+419_255+420del	XP_011525240.1:n.255+419_255+420del
XR_935823.1:n.1533+419_1533+420del
XR_002958313.1:n.1533+419_1533+420del
NM_002250.3:c.255+419_255+420del MANE Select	NP_002241.1:n.255+419_255+420del