Canonical Allele Identifier: CA1622625618

Gene: KCNK17

Genomic Alleles

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

Transcript Alleles

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