Canonical Allele Identifier: CA449812535

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31928027T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960250T>C , CM000668.2:g.31960250T>C	GRCh38
NC_000006.11:g.31928027T>C , CM000668.1:g.31928027T>C	GRCh37
NC_000006.10:g.32036006T>C	NCBI36
NG_032652.1:g.6447T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.267T>C	ENSP00000419905.1:p.Ser89=
ENST00000483553.6:c.267T>C	ENSP00000420332.2:p.Ser89=
ENST00000485349.6:n.308T>C
ENST00000491994.2:c.267T>C	ENSP00000417586.2:p.Ser89=
ENST00000494058.6:n.324T>C
ENST00000697831.1:c.267T>C	ENSP00000513453.1:p.Ser89=
ENST00000697832.1:n.343T>C
ENST00000697833.1:c.267T>C	ENSP00000513454.1:p.Ser89=
ENST00000697834.1:n.319T>C
ENST00000697835.1:c.286T>C	ENSP00000513455.1:p.Ser96Pro
ENST00000697836.1:n.303T>C
ENST00000697837.1:c.267T>C	ENSP00000513456.1:p.Ser89=
ENST00000697838.1:c.132T>C	ENSP00000513457.1:p.Ser44=
ENST00000697839.1:n.289T>C
ENST00000697840.1:c.267T>C	ENSP00000513458.1:p.Ser89=
ENST00000697841.1:n.278T>C
ENST00000697842.1:n.267T>C
ENST00000375394.7:c.267T>C MANE Select	ENSP00000364543.2:p.Ser89=
ENST00000375394.6:c.267T>C	ENSP00000364543.2:p.Ser89=
ENST00000461073.5:c.267T>C	ENSP00000419905.1:p.Ser89=
ENST00000465703.5:n.319T>C
ENST00000474839.5:c.127-791T>C	ENSP00000420470.1:n.127-791T>C
ENST00000488648.5:n.343T>C
ENST00000628157.1:c.127-791T>C	ENSP00000485707.1:n.127-791T>C
NM_006929.4:c.267T>C	NP_008860.4:p.Ser89=
XM_006715168.2:c.267T>C	XP_006715231.1:p.Ser89=
XM_011514815.1:c.267T>C	XP_011513117.1:p.Ser89=
XR_926301.1:n.355T>C
XM_011514815.3:c.267T>C	XP_011513117.1:p.Ser89=
XR_001743586.2:n.303T>C
XR_926301.3:n.303T>C
NM_006929.5:c.267T>C MANE Select	NP_008860.4:p.Ser89=