Canonical Allele Identifier: CA1622625627

Gene: KCNK17

Linked Data

• dbSNP Id: rs1761943598

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39301019T>C , CM000668.2:g.39301019T>C	GRCh38
NC_000006.11:g.39268795T>C , CM000668.1:g.39268795T>C	GRCh37
NC_000006.10:g.39376773T>C	NCBI36
NG_047208.1:g.18443A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373231.9:c.689-1282A>G MANE Select	ENSP00000362328.4:n.689-1282A>G
ENST00000373231.8:c.689-1282A>G	ENSP00000362328.4:n.689-1282A>G
ENST00000453413.2:c.689-496A>G	ENSP00000401271.2:n.689-496A>G
NM_001135111.1:c.689-496A>G	NP_001128583.1:n.689-496A>G
NM_031460.3:c.689-1282A>G	NP_113648.2:n.689-1282A>G
XM_006715239.2:c.689-514A>G	XP_006715302.1:n.689-514A>G
XM_011514973.1:c.398-1282A>G	XP_011513275.1:n.398-1282A>G
NM_031460.4:c.689-1282A>G MANE Select	NP_113648.2:n.689-1282A>G
NM_001135111.2:c.689-496A>G	NP_001128583.1:n.689-496A>G