Canonical Allele Identifier: CA1622627473
Gene: KCNK17 HGNC NCBI

Linked Data

dbSNP Id: rs1762011397
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39305018G>A , CM000668.2:g.39305018G>A GRCh38
NC_000006.11:g.39272794G>A , CM000668.1:g.39272794G>A GRCh37
NC_000006.10:g.39380772G>A NCBI36
NG_047208.1:g.14444C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373231.9:c.353-363C>T MANE Select ENSP00000362328.4:n.353-363C>T
ENST00000373231.8:c.353-363C>T ENSP00000362328.4:n.353-363C>T
ENST00000453413.2:c.353-363C>T ENSP00000401271.2:n.353-363C>T
ENST00000503878.1:n.458-363C>T
NM_001135111.1:c.353-363C>T NP_001128583.1:n.353-363C>T
NM_031460.3:c.353-363C>T NP_113648.2:n.353-363C>T
XM_006715239.2:c.353-363C>T XP_006715302.1:n.353-363C>T
XM_011514973.1:c.62-363C>T XP_011513275.1:n.62-363C>T
NM_031460.4:c.353-363C>T MANE Select NP_113648.2:n.353-363C>T
NM_001135111.2:c.353-363C>T NP_001128583.1:n.353-363C>T
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