Canonical Allele Identifier: CA406098759

Gene: CIC

Linked Data

• ClinVar Variation Id: 451974
• ClinVar RCV Id: RCV000523551
• dbSNP Id: rs1555765916
• MyVariant Identifiers: chr19:g.42791878A>G (hg19) ; chr19:g.42287726A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.42287726A>G , CM000681.2:g.42287726A>G	GRCh38
NC_000019.9:g.42791878A>G , CM000681.1:g.42791878A>G	GRCh37
NC_000019.8:g.47483718A>G	NCBI36
NG_042060.1:g.24190A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684265.1:n.2574A>G
ENST00000681038.1:c.3491A>G MANE Select	ENSP00000505728.1:p.Gln1164Arg
ENST00000160740.7:c.764A>G	ENSP00000160740.3:p.Gln255Arg
ENST00000572681.6:c.3491A>G	ENSP00000459719.1:p.Gln1164Arg
ENST00000575354.6:c.764A>G	ENSP00000458663.2:p.Gln255Arg
NM_001304815.1:c.3491A>G	NP_001291744.1:p.Gln1164Arg
NM_015125.4:c.764A>G	NP_055940.3:p.Gln255Arg
XM_005258673.1:c.764A>G	XP_005258730.1:p.Gln255Arg
XM_005258674.1:c.764A>G	XP_005258731.1:p.Gln255Arg
XM_005258675.1:c.764A>G	XP_005258732.1:p.Gln255Arg
XM_011526660.1:c.3491A>G	XP_011524962.1:p.Gln1164Arg
XM_011526661.1:c.3491A>G	XP_011524963.1:p.Gln1164Arg
XM_011526662.1:c.3491A>G	XP_011524964.1:p.Gln1164Arg
XM_011526663.1:c.3491A>G	XP_011524965.1:p.Gln1164Arg
XM_011526664.1:c.3491A>G	XP_011524966.1:p.Gln1164Arg
XM_011526665.1:c.3491A>G	XP_011524967.1:p.Gln1164Arg
XM_011526666.1:c.3491A>G	XP_011524968.1:p.Gln1164Arg
XM_011526667.1:c.3491A>G	XP_011524969.1:p.Gln1164Arg
XR_935775.1:n.3602A>G
XR_935776.1:n.3602A>G
XR_935777.1:n.3602A>G
XR_935778.1:n.3602A>G
XR_935779.1:n.3602A>G
XM_005258673.2:c.764A>G	XP_005258730.1:p.Gln255Arg
XM_005258674.2:c.764A>G	XP_005258731.1:p.Gln255Arg
XM_005258675.2:c.764A>G	XP_005258732.1:p.Gln255Arg
XM_011526660.2:c.3491A>G	XP_011524962.1:p.Gln1164Arg
XM_011526661.2:c.3491A>G	XP_011524963.1:p.Gln1164Arg
XM_011526662.2:c.3491A>G	XP_011524964.1:p.Gln1164Arg
XM_011526663.2:c.3491A>G	XP_011524965.1:p.Gln1164Arg
XM_011526664.2:c.3491A>G	XP_011524966.1:p.Gln1164Arg
XM_011526665.2:c.3491A>G	XP_011524967.1:p.Gln1164Arg
XM_011526666.2:c.3491A>G	XP_011524968.1:p.Gln1164Arg
XM_011526667.2:c.3491A>G	XP_011524969.1:p.Gln1164Arg
XM_024451432.1:c.3491A>G	XP_024307200.1:p.Gln1164Arg
XM_024451433.1:c.3491A>G	XP_024307201.1:p.Gln1164Arg
XR_002958286.1:n.3601A>G
XR_002958287.1:n.3601A>G
XR_002958288.1:n.3601A>G
XR_002958289.1:n.3601A>G
XR_002958290.1:n.3601A>G
XR_935778.2:n.3601A>G
XR_935779.2:n.3601A>G
NM_001304815.2:c.3491A>G	NP_001291744.1:p.Gln1164Arg
NM_001379480.1:c.3491A>G	NP_001366409.1:p.Gln1164Arg
NM_001379482.1:c.3491A>G	NP_001366411.1:p.Gln1164Arg
NM_001379484.1:c.764A>G	NP_001366413.1:p.Gln255Arg
NM_001379485.1:c.764A>G	NP_001366414.1:p.Gln255Arg
NM_001386298.1:c.3491A>G MANE Select	NP_001373227.1:p.Gln1164Arg
NM_015125.5:c.764A>G	NP_055940.3:p.Gln255Arg