Canonical Allele Identifier: CA2585562856

Gene: KCNN4

Linked Data

• gnomAD v4: 19-43776478-GTGAGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776482_43776486del , CM000681.2:g.43776482_43776486del	GRCh38
NC_000019.9:g.44280634_44280638del , CM000681.1:g.44280634_44280638del	GRCh37
NC_000019.8:g.48972474_48972478del	NCBI36
NG_052672.1:g.10657_10661del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+58_255+62del MANE Select	ENSP00000496939.1:n.255+58_255+62del
ENST00000262888.7:c.255+58_255+62del	ENSP00000262888.3:n.255+58_255+62del
ENST00000599107.1:n.286+58_286+62del
ENST00000599720.5:c.159+4220_159+4224del	ENSP00000472513.1:n.159+4220_159+4224del
ENST00000615047.4:c.70+58_70+62del	ENSP00000485014.1:n.70+58_70+62del
NM_002250.2:c.255+58_255+62del	NP_002241.1:n.255+58_255+62del
XM_005258882.2:c.160-1864_160-1860del	XP_005258939.1:n.160-1864_160-1860del
XM_005258883.2:c.70+58_70+62del	XP_005258940.1:n.70+58_70+62del
XM_011526938.1:c.255+58_255+62del	XP_011525240.1:n.255+58_255+62del
XR_935823.1:n.1533+58_1533+62del
XR_002958313.1:n.1533+58_1533+62del
NM_002250.3:c.255+58_255+62del MANE Select	NP_002241.1:n.255+58_255+62del