Canonical Allele Identifier: CA1622625615
Gene: KCNK17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39300990C= , CM000668.2:g.39300990C= GRCh38
NC_000006.11:g.39268766C= , CM000668.1:g.39268766C= GRCh37
NC_000006.10:g.39376744C= NCBI36
NG_047208.1:g.18472G=

Transcript Alleles

HGVS Amino-acid change
ENST00000373231.9:c.689-1253G= MANE Select ENSP00000362328.4:n.689-1253G=
ENST00000373231.8:c.689-1253G= ENSP00000362328.4:n.689-1253G=
ENST00000453413.2:c.689-467G= ENSP00000401271.2:n.689-467G=
NM_001135111.1:c.689-467G= NP_001128583.1:n.689-467G=
NM_031460.3:c.689-1253G= NP_113648.2:n.689-1253G=
XM_006715239.2:c.689-485G= XP_006715302.1:n.689-485G=
XM_011514973.1:c.398-1253G= XP_011513275.1:n.398-1253G=
NM_031460.4:c.689-1253G= MANE Select NP_113648.2:n.689-1253G=
NM_001135111.2:c.689-467G= NP_001128583.1:n.689-467G=
Search 100 bp 5'
Search 100 bp 3'