Canonical Allele Identifier: CA824540114

Gene: KCNK17

Linked Data

• dbSNP Id: rs1364120082
• gnomAD v3: 6-39305023-G-C
• gnomAD v4: 6-39305023-G-C
• MyVariant Identifiers: chr6:g.39272799G>C (hg19) ; chr6:g.39305023G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39305023G>C , CM000668.2:g.39305023G>C	GRCh38
NC_000006.11:g.39272799G>C , CM000668.1:g.39272799G>C	GRCh37
NC_000006.10:g.39380777G>C	NCBI36
NG_047208.1:g.14439C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373231.9:c.353-368C>G MANE Select	ENSP00000362328.4:n.353-368C>G
ENST00000373231.8:c.353-368C>G	ENSP00000362328.4:n.353-368C>G
ENST00000453413.2:c.353-368C>G	ENSP00000401271.2:n.353-368C>G
ENST00000503878.1:n.458-368C>G
NM_001135111.1:c.353-368C>G	NP_001128583.1:n.353-368C>G
NM_031460.3:c.353-368C>G	NP_113648.2:n.353-368C>G
XM_006715239.2:c.353-368C>G	XP_006715302.1:n.353-368C>G
XM_011514973.1:c.62-368C>G	XP_011513275.1:n.62-368C>G
NM_031460.4:c.353-368C>G MANE Select	NP_113648.2:n.353-368C>G
NM_001135111.2:c.353-368C>G	NP_001128583.1:n.353-368C>G