Canonical Allele Identifier: CA396067346

Gene: KATNB1

Linked Data

• MyVariant Identifiers: chr16:g.57785561C>A (hg19) ; chr16:g.57751649C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57751649C>A , CM000678.2:g.57751649C>A	GRCh38
NC_000016.9:g.57785561C>A , CM000678.1:g.57785561C>A	GRCh37
NC_000016.8:g.56343062C>A	NCBI36
NG_046947.1:g.20930C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379661.8:c.441C>A MANE Select	ENSP00000368982.3:p.Ser147Arg
ENST00000379661.7:c.441C>A	ENSP00000368982.3:p.Ser147Arg
ENST00000562592.5:c.441C>A	ENSP00000455350.1:p.Ser147Arg
ENST00000563127.1:n.493C>A
ENST00000566611.5:n.960C>A
ENST00000566726.5:c.453C>A	ENSP00000455270.1:p.Ser151Arg
ENST00000569627.1:c.340C>A	ENSP00000457046.1:p.Pro114Thr
NM_005886.2:c.441C>A	NP_005877.2:p.Ser147Arg
XM_005255772.3:c.441C>A	XP_005255829.1:p.Ser147Arg
XM_006721121.2:c.441C>A	XP_006721184.1:p.Ser147Arg
XM_006721122.2:c.441C>A	XP_006721185.1:p.Ser147Arg
XM_006721123.2:c.441C>A	XP_006721186.1:p.Ser147Arg
XM_011522810.1:c.441C>A	XP_011521112.1:p.Ser147Arg
XM_005255772.5:c.441C>A	XP_005255829.1:p.Ser147Arg
XM_006721121.4:c.441C>A	XP_006721184.1:p.Ser147Arg
XM_006721123.4:c.441C>A	XP_006721186.1:p.Ser147Arg
XM_011522810.2:c.441C>A	XP_011521112.1:p.Ser147Arg
XM_017022860.2:c.441C>A	XP_016878349.1:p.Ser147Arg
XM_017022861.1:c.441C>A	XP_016878350.1:p.Ser147Arg
XM_017022862.1:c.441C>A	XP_016878351.1:p.Ser147Arg
XM_017022863.1:c.441C>A	XP_016878352.1:p.Ser147Arg
XM_017022864.1:c.441C>A	XP_016878353.1:p.Ser147Arg
NM_005886.3:c.441C>A MANE Select	NP_005877.2:p.Ser147Arg