Canonical Allele Identifier: CA3729098

Gene: SKIC2

Linked Data

• ClinVar Variation Id: 2956642
• ClinVar RCV Id: RCV003816353
• dbSNP Id: rs140500193
• ExAC: 6:31928015 G / A
• gnomAD v2: 6-31928015-G-A
• gnomAD v3: 6-31960238-G-A
• gnomAD v4: 6-31960238-G-A
• MyVariant Identifiers: chr6:g.31928015G>A (hg19) ; chr6:g.31960238G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960238G>A , CM000668.2:g.31960238G>A	GRCh38
NC_000006.11:g.31928015G>A , CM000668.1:g.31928015G>A	GRCh37
NC_000006.10:g.32035994G>A	NCBI36
NG_032652.1:g.6435G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.255G>A	ENSP00000419905.1:p.Thr85=
ENST00000483553.6:c.255G>A	ENSP00000420332.2:p.Thr85=
ENST00000485349.6:n.296G>A
ENST00000491994.2:c.255G>A	ENSP00000417586.2:p.Thr85=
ENST00000494058.6:n.312G>A
ENST00000697831.1:c.255G>A	ENSP00000513453.1:p.Thr85=
ENST00000697832.1:n.331G>A
ENST00000697833.1:c.255G>A	ENSP00000513454.1:p.Thr85=
ENST00000697834.1:n.307G>A
ENST00000697835.1:c.274G>A	ENSP00000513455.1:p.Gly92Arg
ENST00000697836.1:n.291G>A
ENST00000697837.1:c.255G>A	ENSP00000513456.1:p.Thr85=
ENST00000697838.1:c.120G>A	ENSP00000513457.1:p.Thr40=
ENST00000697839.1:n.277G>A
ENST00000697840.1:c.255G>A	ENSP00000513458.1:p.Thr85=
ENST00000697841.1:n.266G>A
ENST00000697842.1:n.255G>A
ENST00000375394.7:c.255G>A MANE Select	ENSP00000364543.2:p.Thr85=
ENST00000375394.6:c.255G>A	ENSP00000364543.2:p.Thr85=
ENST00000461073.5:c.255G>A	ENSP00000419905.1:p.Thr85=
ENST00000465703.5:n.307G>A
ENST00000474839.5:c.127-803G>A	ENSP00000420470.1:n.127-803G>A
ENST00000488648.5:n.331G>A
ENST00000628157.1:c.127-803G>A	ENSP00000485707.1:n.127-803G>A
NM_006929.4:c.255G>A	NP_008860.4:p.Thr85=
XM_006715168.2:c.255G>A	XP_006715231.1:p.Thr85=
XM_011514815.1:c.255G>A	XP_011513117.1:p.Thr85=
XR_926301.1:n.343G>A
XM_011514815.3:c.255G>A	XP_011513117.1:p.Thr85=
XR_001743586.2:n.291G>A
XR_926301.3:n.291G>A
NM_006929.5:c.255G>A MANE Select	NP_008860.4:p.Thr85=