Canonical Allele Identifier: CA137606808

Gene: KCNK5

Linked Data

• dbSNP Id: rs34911577
• MyVariant Identifiers: chr6:g.39183774_39183775insG (hg19) ; chr6:g.39215998_39215999insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39216002dup , CM000668.2:g.39216002dup	GRCh38
NC_000006.11:g.39183778dup , CM000668.1:g.39183778dup	GRCh37
NC_000006.10:g.39291756dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359534.4:c.186+12927dup MANE Select	ENSP00000352527.3:n.186+12927dup
ENST00000359534.3:c.186+12927dup	ENSP00000352527.3:n.186+12927dup
NM_003740.3:c.186+12927dup	NP_003731.1:n.186+12927dup
XM_005249456.1:c.186+12927dup	XP_005249513.1:n.186+12927dup
NM_003740.4:c.186+12927dup MANE Select	NP_003731.1:n.186+12927dup