Canonical Allele Identifier: CA362971782

Gene: KIAA0319

Linked Data

• MyVariant Identifiers: chr6:g.24596460A>G (hg19) ; chr6:g.24596232A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24596232A>G , CM000668.2:g.24596232A>G	GRCh38
NC_000006.11:g.24596460A>G , CM000668.1:g.24596460A>G	GRCh37
NC_000006.10:g.24704439A>G	NCBI36
NG_016206.1:g.54924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378214.8:c.442T>C MANE Select	ENSP00000367459.3:p.Trp148Arg
ENST00000378214.7:c.442T>C	ENSP00000367459.3:p.Trp148Arg
ENST00000430948.6:c.307T>C	ENSP00000401086.2:p.Trp103Arg
ENST00000535378.5:c.415T>C	ENSP00000442403.1:p.Trp139Arg
ENST00000537886.5:c.442T>C	ENSP00000439700.1:p.Trp148Arg
ENST00000543707.2:c.442T>C	ENSP00000437656.1:p.Trp148Arg
NM_001168374.1:c.415T>C	NP_001161846.1:p.Trp139Arg
NM_001168375.1:c.442T>C	NP_001161847.1:p.Trp148Arg
NM_001168376.1:c.307T>C	NP_001161848.1:p.Trp103Arg
NM_001168377.1:c.442T>C	NP_001161849.1:p.Trp148Arg
NM_014809.3:c.442T>C	NP_055624.2:p.Trp148Arg
XM_006715288.2:c.-15T>C	XP_006715351.1:n.-15T>C
XM_011515022.1:c.460T>C	XP_011513324.1:p.Trp154Arg
XM_011515023.1:c.460T>C	XP_011513325.1:p.Trp154Arg
XM_011515024.1:c.460T>C	XP_011513326.1:p.Trp154Arg
XM_011515025.1:c.442T>C	XP_011513327.1:p.Trp148Arg
XM_011515026.1:c.307T>C	XP_011513328.1:p.Trp103Arg
NM_001350403.1:c.442T>C	NP_001337332.1:p.Trp148Arg
NM_001350404.1:c.424T>C	NP_001337333.1:p.Trp142Arg
NM_001350405.1:c.442T>C	NP_001337334.1:p.Trp148Arg
NM_001350406.1:c.307T>C	NP_001337335.1:p.Trp103Arg
NM_001350407.1:c.442T>C	NP_001337336.1:p.Trp148Arg
NM_001350408.1:c.442T>C	NP_001337337.1:p.Trp148Arg
NM_001350409.1:c.-15T>C	NP_001337338.1:n.-15T>C
NM_001350410.1:c.-15T>C	NP_001337339.1:n.-15T>C
XM_011515026.3:c.307T>C	XP_011513328.1:p.Trp103Arg
XM_017011541.1:c.415T>C	XP_016867030.1:p.Trp139Arg
XM_017011542.2:c.442T>C	XP_016867031.1:p.Trp148Arg
XM_017011544.1:c.442T>C	XP_016867033.1:p.Trp148Arg
XM_017011546.2:c.442T>C	XP_016867035.1:p.Trp148Arg
XM_017011547.1:c.442T>C	XP_016867036.1:p.Trp148Arg
XM_017011550.1:c.442T>C	XP_016867039.1:p.Trp148Arg
XM_017011551.1:c.442T>C	XP_016867040.1:p.Trp148Arg
XR_001743779.1:n.685T>C
XR_001743780.1:n.685T>C
NM_014809.4:c.442T>C MANE Select	NP_055624.2:p.Trp148Arg
NM_001168375.2:c.442T>C	NP_001161847.1:p.Trp148Arg
NM_001350403.2:c.442T>C	NP_001337332.1:p.Trp148Arg
NM_001350404.2:c.424T>C	NP_001337333.1:p.Trp142Arg
NM_001350405.2:c.442T>C	NP_001337334.1:p.Trp148Arg
NM_001350406.2:c.307T>C	NP_001337335.1:p.Trp103Arg
NM_001350407.2:c.442T>C	NP_001337336.1:p.Trp148Arg
NM_001350408.2:c.442T>C	NP_001337337.1:p.Trp148Arg
NM_001350409.2:c.-15T>C	NP_001337338.1:n.-15T>C
NM_001350410.2:c.-15T>C	NP_001337339.1:n.-15T>C
NM_001168374.2:c.415T>C	NP_001161846.1:p.Trp139Arg
NM_001168376.2:c.307T>C	NP_001161848.1:p.Trp103Arg
NM_001168377.2:c.442T>C	NP_001161849.1:p.Trp148Arg