Canonical Allele Identifier: CA1622582619
Gene: KCNK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39216060A= , CM000668.2:g.39216060A= GRCh38
NC_000006.11:g.39183836A= , CM000668.1:g.39183836A= GRCh37
NC_000006.10:g.39291814A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359534.4:c.186+12866T= MANE Select ENSP00000352527.3:n.186+12866T=
ENST00000359534.3:c.186+12866T= ENSP00000352527.3:n.186+12866T=
NM_003740.3:c.186+12866T= NP_003731.1:n.186+12866T=
XM_005249456.1:c.186+12866T= XP_005249513.1:n.186+12866T=
NM_003740.4:c.186+12866T= MANE Select NP_003731.1:n.186+12866T=