Canonical Allele Identifier: CA137606781
Gene: KCNK5 HGNC NCBI

Linked Data

dbSNP Id: rs902612871
gnomAD v3: 6-39215932-TTAACA-T
gnomAD v4: 6-39215932-TTAACA-T
MyVariant Identifiers: chr6:g.39183709_39183713del (hg19) chr6:g.39215933_39215937del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39215933_39215937del , CM000668.2:g.39215933_39215937del GRCh38
NC_000006.11:g.39183709_39183713del , CM000668.1:g.39183709_39183713del GRCh37
NC_000006.10:g.39291687_39291691del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359534.4:c.186+12989_186+12993del MANE Select ENSP00000352527.3:n.186+12989_186+12993del
ENST00000359534.3:c.186+12989_186+12993del ENSP00000352527.3:n.186+12989_186+12993del
NM_003740.3:c.186+12989_186+12993del NP_003731.1:n.186+12989_186+12993del
XM_005249456.1:c.186+12989_186+12993del XP_005249513.1:n.186+12989_186+12993del
NM_003740.4:c.186+12989_186+12993del MANE Select NP_003731.1:n.186+12989_186+12993del
Search 100 bp 5'
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