Canonical Allele Identifier: CA2224758788

Gene: KATNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57751651A= , CM000678.2:g.57751651A=	GRCh38
NC_000016.9:g.57785563A= , CM000678.1:g.57785563A=	GRCh37
NC_000016.8:g.56343064A=	NCBI36
NG_046947.1:g.20932A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379661.8:c.443A= MANE Select	ENSP00000368982.3:p.Gln148=
ENST00000379661.7:c.443A=	ENSP00000368982.3:p.Gln148=
ENST00000562592.5:c.443A=	ENSP00000455350.1:p.Gln148=
ENST00000563127.1:n.495A=
ENST00000566611.5:n.962A=
ENST00000566726.5:c.455A=	ENSP00000455270.1:p.Gln152=
ENST00000569627.1:c.342A=	ENSP00000457046.1:p.Pro114=
NM_005886.2:c.443A=	NP_005877.2:p.Gln148=
XM_005255772.3:c.443A=	XP_005255829.1:p.Gln148=
XM_006721121.2:c.443A=	XP_006721184.1:p.Gln148=
XM_006721122.2:c.443A=	XP_006721185.1:p.Gln148=
XM_006721123.2:c.443A=	XP_006721186.1:p.Gln148=
XM_011522810.1:c.443A=	XP_011521112.1:p.Gln148=
XM_005255772.5:c.443A=	XP_005255829.1:p.Gln148=
XM_006721121.4:c.443A=	XP_006721184.1:p.Gln148=
XM_006721123.4:c.443A=	XP_006721186.1:p.Gln148=
XM_011522810.2:c.443A=	XP_011521112.1:p.Gln148=
XM_017022860.2:c.443A=	XP_016878349.1:p.Gln148=
XM_017022861.1:c.443A=	XP_016878350.1:p.Gln148=
XM_017022862.1:c.443A=	XP_016878351.1:p.Gln148=
XM_017022863.1:c.443A=	XP_016878352.1:p.Gln148=
XM_017022864.1:c.443A=	XP_016878353.1:p.Gln148=
NM_005886.3:c.443A= MANE Select	NP_005877.2:p.Gln148=