Canonical Allele Identifier: CA2585562837
Gene: KCNN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43776466_43776468dup , CM000681.2:g.43776466_43776468dup GRCh38
NC_000019.9:g.44280618_44280620dup , CM000681.1:g.44280618_44280620dup GRCh37
NC_000019.8:g.48972458_48972460dup NCBI36
NG_052672.1:g.10684_10686dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000648319.1:c.255+85_255+87dup MANE Select ENSP00000496939.1:n.255+85_255+87dup
ENST00000262888.7:c.255+85_255+87dup ENSP00000262888.3:n.255+85_255+87dup
ENST00000599107.1:n.286+85_286+87dup
ENST00000599720.5:c.159+4247_159+4249dup ENSP00000472513.1:n.159+4247_159+4249dup
ENST00000615047.4:c.70+85_70+87dup ENSP00000485014.1:n.70+85_70+87dup
NM_002250.2:c.255+85_255+87dup NP_002241.1:n.255+85_255+87dup
XM_005258882.2:c.160-1837_160-1835dup XP_005258939.1:n.160-1837_160-1835dup
XM_005258883.2:c.70+85_70+87dup XP_005258940.1:n.70+85_70+87dup
XM_011526938.1:c.255+85_255+87dup XP_011525240.1:n.255+85_255+87dup
XR_935823.1:n.1533+85_1533+87dup
XR_002958313.1:n.1533+85_1533+87dup
NM_002250.3:c.255+85_255+87dup MANE Select NP_002241.1:n.255+85_255+87dup