Canonical Allele Identifier: CA1600349559

Gene: KCNMB1 KCNIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.170383792C= , CM000667.2:g.170383792C=	GRCh38
NC_000005.9:g.169810796C= , CM000667.1:g.169810796C=	GRCh37
NC_000005.8:g.169743374C=	NCBI36
NG_011452.2:g.10843G=
NG_011538.1:g.34916C=
NG_011538.2:g.34916C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274629.9:c.193G= (KCNMB1) MANE Select	ENSP00000274629.3:p.Glu65=
ENST00000274629.8:c.193G= (KCNMB1)	ENSP00000274629.3:p.Glu65=
ENST00000377360.8:c.88+29828C= (KCNIP1)	ENSP00000366577.4:n.88+29828C=
ENST00000517344.1:c.88+29828C= (KCNIP1)	ENSP00000431053.1:n.88+29828C=
ENST00000518527.1:n.478+29828C= (KCNIP1)
ENST00000521859.1:c.193G= (KCNMB1)	ENSP00000427940.1:p.Glu65=
NM_001034838.2:c.88+29828C= (KCNIP1)	NP_001030010.1:n.88+29828C=
NM_004137.3:c.193G= (KCNMB1)	NP_004128.1:p.Glu65=
XM_006714861.1:c.-1+29828C= (KCNIP1)	XP_006714924.1:n.-1+29828C=
XM_011534539.1:c.88+29828C= (KCNIP1)	XP_011532841.1:n.88+29828C=
XM_017009407.1:c.88+29828C= (KCNIP1)	XP_016864896.1:n.88+29828C=
XM_017009408.1:c.88+29828C= (KCNIP1)	XP_016864897.1:n.88+29828C=
NM_004137.4:c.193G= (KCNMB1) MANE Select	NP_004128.1:p.Glu65=
NM_001034838.3:c.88+29828C= (KCNIP1)	NP_001030010.1:n.88+29828C=