Canonical Allele Identifier: CA137633203
Gene: KCNK17 HGNC NCBI

Linked Data

dbSNP Id: rs545153495
gnomAD v3: 6-39305038-G-T
gnomAD v4: 6-39305038-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39305038G>T , CM000668.2:g.39305038G>T GRCh38
NC_000006.11:g.39272814G>T , CM000668.1:g.39272814G>T GRCh37
NC_000006.10:g.39380792G>T NCBI36
NG_047208.1:g.14424C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373231.9:c.353-383C>A MANE Select ENSP00000362328.4:n.353-383C>A
ENST00000373231.8:c.353-383C>A ENSP00000362328.4:n.353-383C>A
ENST00000453413.2:c.353-383C>A ENSP00000401271.2:n.353-383C>A
ENST00000503878.1:n.458-383C>A
NM_001135111.1:c.353-383C>A NP_001128583.1:n.353-383C>A
NM_031460.3:c.353-383C>A NP_113648.2:n.353-383C>A
XM_006715239.2:c.353-383C>A XP_006715302.1:n.353-383C>A
XM_011514973.1:c.62-383C>A XP_011513275.1:n.62-383C>A
NM_031460.4:c.353-383C>A MANE Select NP_113648.2:n.353-383C>A
NM_001135111.2:c.353-383C>A NP_001128583.1:n.353-383C>A