Canonical Allele Identifier: CA2337655663
Gene: KCNN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.43776295_43776297delinsACT , CM000681.2:g.43776295_43776297delinsACT GRCh38
NC_000019.9:g.44280447_44280449delinsACT , CM000681.1:g.44280447_44280449delinsACT GRCh37
NC_000019.8:g.48972287_48972289delinsACT NCBI36
NG_052672.1:g.10843_10845delinsAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000648319.1:c.255+244_255+246delinsAGT MANE Select ENSP00000496939.1:n.255+244_255+246delinsAGT
ENST00000262888.7:c.255+244_255+246delinsAGT ENSP00000262888.3:n.255+244_255+246delinsAGT
ENST00000599107.1:n.286+244_286+246delinsAGT
ENST00000599720.5:c.160-4194_160-4192delinsAGT ENSP00000472513.1:n.160-4194_160-4192delinsAGT
ENST00000615047.4:c.70+244_70+246delinsAGT ENSP00000485014.1:n.70+244_70+246delinsAGT
NM_002250.2:c.255+244_255+246delinsAGT NP_002241.1:n.255+244_255+246delinsAGT
XM_005258882.2:c.160-1678_160-1676delinsAGT XP_005258939.1:n.160-1678_160-1676delinsAGT
XM_005258883.2:c.70+244_70+246delinsAGT XP_005258940.1:n.70+244_70+246delinsAGT
XM_011526938.1:c.255+244_255+246delinsAGT XP_011525240.1:n.255+244_255+246delinsAGT
XR_935823.1:n.1533+244_1533+246delinsAGT
XR_002958313.1:n.1533+244_1533+246delinsAGT
NM_002250.3:c.255+244_255+246delinsAGT MANE Select NP_002241.1:n.255+244_255+246delinsAGT