Canonical Allele Identifier: CA1622625619

Gene: KCNK17

Linked Data

• dbSNP Id: rs1761943383

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39300993A>G , CM000668.2:g.39300993A>G	GRCh38
NC_000006.11:g.39268769A>G , CM000668.1:g.39268769A>G	GRCh37
NC_000006.10:g.39376747A>G	NCBI36
NG_047208.1:g.18469T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373231.9:c.689-1256T>C MANE Select	ENSP00000362328.4:n.689-1256T>C
ENST00000373231.8:c.689-1256T>C	ENSP00000362328.4:n.689-1256T>C
ENST00000453413.2:c.689-470T>C	ENSP00000401271.2:n.689-470T>C
NM_001135111.1:c.689-470T>C	NP_001128583.1:n.689-470T>C
NM_031460.3:c.689-1256T>C	NP_113648.2:n.689-1256T>C
XM_006715239.2:c.689-488T>C	XP_006715302.1:n.689-488T>C
XM_011514973.1:c.398-1256T>C	XP_011513275.1:n.398-1256T>C
NM_031460.4:c.689-1256T>C MANE Select	NP_113648.2:n.689-1256T>C
NM_001135111.2:c.689-470T>C	NP_001128583.1:n.689-470T>C