Canonical Allele Identifier: CA362971389

Gene: KIAA0319

Linked Data

• MyVariant Identifiers: chr6:g.24596371T>A (hg19) ; chr6:g.24596143T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24596143T>A , CM000668.2:g.24596143T>A	GRCh38
NC_000006.11:g.24596371T>A , CM000668.1:g.24596371T>A	GRCh37
NC_000006.10:g.24704350T>A	NCBI36
NG_016206.1:g.55013A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378214.8:c.531A>T MANE Select	ENSP00000367459.3:p.Arg177Ser
ENST00000378214.7:c.531A>T	ENSP00000367459.3:p.Arg177Ser
ENST00000430948.6:c.396A>T	ENSP00000401086.2:p.Arg132Ser
ENST00000535378.5:c.504A>T	ENSP00000442403.1:p.Arg168Ser
ENST00000537886.5:c.531A>T	ENSP00000439700.1:p.Arg177Ser
ENST00000543707.2:c.531A>T	ENSP00000437656.1:p.Arg177Ser
NM_001168374.1:c.504A>T	NP_001161846.1:p.Arg168Ser
NM_001168375.1:c.531A>T	NP_001161847.1:p.Arg177Ser
NM_001168376.1:c.396A>T	NP_001161848.1:p.Arg132Ser
NM_001168377.1:c.531A>T	NP_001161849.1:p.Arg177Ser
NM_014809.3:c.531A>T	NP_055624.2:p.Arg177Ser
XM_006715288.2:c.75A>T	XP_006715351.1:p.Arg25Ser
XM_011515022.1:c.549A>T	XP_011513324.1:p.Arg183Ser
XM_011515023.1:c.549A>T	XP_011513325.1:p.Arg183Ser
XM_011515024.1:c.549A>T	XP_011513326.1:p.Arg183Ser
XM_011515025.1:c.531A>T	XP_011513327.1:p.Arg177Ser
XM_011515026.1:c.396A>T	XP_011513328.1:p.Arg132Ser
NM_001350403.1:c.531A>T	NP_001337332.1:p.Arg177Ser
NM_001350404.1:c.513A>T	NP_001337333.1:p.Arg171Ser
NM_001350405.1:c.531A>T	NP_001337334.1:p.Arg177Ser
NM_001350406.1:c.396A>T	NP_001337335.1:p.Arg132Ser
NM_001350407.1:c.531A>T	NP_001337336.1:p.Arg177Ser
NM_001350408.1:c.531A>T	NP_001337337.1:p.Arg177Ser
NM_001350409.1:c.75A>T	NP_001337338.1:p.Arg25Ser
NM_001350410.1:c.75A>T	NP_001337339.1:p.Arg25Ser
XM_011515026.3:c.396A>T	XP_011513328.1:p.Arg132Ser
XM_017011541.1:c.504A>T	XP_016867030.1:p.Arg168Ser
XM_017011542.2:c.531A>T	XP_016867031.1:p.Arg177Ser
XM_017011544.1:c.531A>T	XP_016867033.1:p.Arg177Ser
XM_017011546.2:c.531A>T	XP_016867035.1:p.Arg177Ser
XM_017011547.1:c.531A>T	XP_016867036.1:p.Arg177Ser
XM_017011550.1:c.531A>T	XP_016867039.1:p.Arg177Ser
XM_017011551.1:c.531A>T	XP_016867040.1:p.Arg177Ser
XR_001743779.1:n.774A>T
XR_001743780.1:n.774A>T
NM_014809.4:c.531A>T MANE Select	NP_055624.2:p.Arg177Ser
NM_001168375.2:c.531A>T	NP_001161847.1:p.Arg177Ser
NM_001350403.2:c.531A>T	NP_001337332.1:p.Arg177Ser
NM_001350404.2:c.513A>T	NP_001337333.1:p.Arg171Ser
NM_001350405.2:c.531A>T	NP_001337334.1:p.Arg177Ser
NM_001350406.2:c.396A>T	NP_001337335.1:p.Arg132Ser
NM_001350407.2:c.531A>T	NP_001337336.1:p.Arg177Ser
NM_001350408.2:c.531A>T	NP_001337337.1:p.Arg177Ser
NM_001350409.2:c.75A>T	NP_001337338.1:p.Arg25Ser
NM_001350410.2:c.75A>T	NP_001337339.1:p.Arg25Ser
NM_001168374.2:c.504A>T	NP_001161846.1:p.Arg168Ser
NM_001168376.2:c.396A>T	NP_001161848.1:p.Arg132Ser
NM_001168377.2:c.531A>T	NP_001161849.1:p.Arg177Ser