Canonical Allele Identifier: CA2585562844

Gene: KCNN4

Linked Data

• gnomAD v4: 19-43776463-AGGAGGGTGGAAAGTGTGAGCTGACAGGGCGCTGAGGGGGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.43776470_43776510del , CM000681.2:g.43776470_43776510del	GRCh38
NC_000019.9:g.44280622_44280662del , CM000681.1:g.44280622_44280662del	GRCh37
NC_000019.8:g.48972462_48972502del	NCBI36
NG_052672.1:g.10636_10676del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648319.1:c.255+37_255+77del MANE Select	ENSP00000496939.1:n.255+37_255+77del
ENST00000262888.7:c.255+37_255+77del	ENSP00000262888.3:n.255+37_255+77del
ENST00000599107.1:n.286+37_286+77del
ENST00000599720.5:c.159+4199_159+4239del	ENSP00000472513.1:n.159+4199_159+4239del
ENST00000615047.4:c.70+37_70+77del	ENSP00000485014.1:n.70+37_70+77del
NM_002250.2:c.255+37_255+77del	NP_002241.1:n.255+37_255+77del
XM_005258882.2:c.160-1885_160-1845del	XP_005258939.1:n.160-1885_160-1845del
XM_005258883.2:c.70+37_70+77del	XP_005258940.1:n.70+37_70+77del
XM_011526938.1:c.255+37_255+77del	XP_011525240.1:n.255+37_255+77del
XR_935823.1:n.1533+37_1533+77del
XR_002958313.1:n.1533+37_1533+77del
NM_002250.3:c.255+37_255+77del MANE Select	NP_002241.1:n.255+37_255+77del