Canonical Allele Identifier: CA1622627492

Gene: KCNK17

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39305063T= , CM000668.2:g.39305063T=	GRCh38
NC_000006.11:g.39272839T= , CM000668.1:g.39272839T=	GRCh37
NC_000006.10:g.39380817T=	NCBI36
NG_047208.1:g.14399A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373231.9:c.353-408A= MANE Select	ENSP00000362328.4:n.353-408A=
ENST00000373231.8:c.353-408A=	ENSP00000362328.4:n.353-408A=
ENST00000453413.2:c.353-408A=	ENSP00000401271.2:n.353-408A=
ENST00000503878.1:n.458-408A=
NM_001135111.1:c.353-408A=	NP_001128583.1:n.353-408A=
NM_031460.3:c.353-408A=	NP_113648.2:n.353-408A=
XM_006715239.2:c.353-408A=	XP_006715302.1:n.353-408A=
XM_011514973.1:c.62-408A=	XP_011513275.1:n.62-408A=
NM_031460.4:c.353-408A= MANE Select	NP_113648.2:n.353-408A=
NM_001135111.2:c.353-408A=	NP_001128583.1:n.353-408A=