Canonical Allele Identifier: CA2388855870

Gene: KCNJ15

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38299437T= , CM000683.2:g.38299437T=	GRCh38
NC_000021.8:g.39671359T= , CM000683.1:g.39671359T=	GRCh37
NC_000021.7:g.38593229T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398938.7:c.176T= MANE Select	ENSP00000381911.2:p.Ile59=
ENST00000328656.8:c.176T=	ENSP00000331698.3:p.Ile59=
ENST00000398925.5:c.176T=	ENSP00000381899.1:p.Ile59=
ENST00000398927.1:c.176T=	ENSP00000381901.1:p.Ile59=
ENST00000398928.5:c.176T=	ENSP00000381902.1:p.Ile59=
ENST00000398930.5:c.176T=	ENSP00000381904.1:p.Ile59=
ENST00000398932.5:c.176T=	ENSP00000381905.1:p.Ile59=
ENST00000398934.5:c.176T=	ENSP00000381907.1:p.Ile59=
ENST00000398938.6:c.176T=	ENSP00000381911.2:p.Ile59=
ENST00000419868.1:c.176T=	ENSP00000400849.1:p.Ile59=
ENST00000438657.5:c.176T=	ENSP00000414487.1:p.Ile59=
ENST00000612702.4:c.176T=	ENSP00000484960.1:p.Ile59=
ENST00000613499.4:c.176T=	ENSP00000479100.1:p.Ile59=
NM_001276435.1:c.176T=	NP_001263364.1:p.Ile59=
NM_001276436.1:c.176T=	NP_001263365.1:p.Ile59=
NM_001276437.1:c.176T=	NP_001263366.1:p.Ile59=
NM_001276438.1:c.176T=	NP_001263367.1:p.Ile59=
NM_001276439.1:c.176T=	NP_001263368.1:p.Ile59=
NM_002243.4:c.176T=	NP_002234.2:p.Ile59=
NM_170736.2:c.176T=	NP_733932.1:p.Ile59=
NM_170737.2:c.176T=	NP_733933.1:p.Ile59=
XM_005260975.2:c.176T=	XP_005261032.1:p.Ile59=
XM_006724002.2:c.176T=	XP_006724065.1:p.Ile59=
XM_011529560.1:c.176T=	XP_011527862.1:p.Ile59=
XM_011529561.1:c.176T=	XP_011527863.1:p.Ile59=
XM_011529560.2:c.176T=	XP_011527862.1:p.Ile59=
XM_011529561.2:c.176T=	XP_011527863.1:p.Ile59=
XM_017028343.1:c.176T=	XP_016883832.1:p.Ile59=
XM_017028344.1:c.176T=	XP_016883833.1:p.Ile59=
XM_017028345.1:c.176T=	XP_016883834.1:p.Ile59=
NM_170736.3:c.176T= MANE Select	NP_733932.1:p.Ile59=
NM_001276437.2:c.176T=	NP_001263366.1:p.Ile59=
NM_001276438.2:c.176T=	NP_001263367.1:p.Ile59=
NM_001276439.2:c.176T=	NP_001263368.1:p.Ile59=
NM_002243.5:c.176T=	NP_002234.2:p.Ile59=
NM_001276435.2:c.176T=	NP_001263364.1:p.Ile59=
NM_001276436.2:c.176T=	NP_001263365.1:p.Ile59=
NM_170737.3:c.176T=	NP_733933.1:p.Ile59=