Canonical Allele Identifier: CA1622582532
Gene: KCNK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39215908T= , CM000668.2:g.39215908T= GRCh38
NC_000006.11:g.39183684T= , CM000668.1:g.39183684T= GRCh37
NC_000006.10:g.39291662T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359534.4:c.186+13018A= MANE Select ENSP00000352527.3:n.186+13018A=
ENST00000359534.3:c.186+13018A= ENSP00000352527.3:n.186+13018A=
NM_003740.3:c.186+13018A= NP_003731.1:n.186+13018A=
XM_005249456.1:c.186+13018A= XP_005249513.1:n.186+13018A=
NM_003740.4:c.186+13018A= MANE Select NP_003731.1:n.186+13018A=