Canonical Allele Identifier: CA363435623

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31928023G>C (hg19) ; chr6:g.31960246G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960246G>C , CM000668.2:g.31960246G>C	GRCh38
NC_000006.11:g.31928023G>C , CM000668.1:g.31928023G>C	GRCh37
NC_000006.10:g.32036002G>C	NCBI36
NG_032652.1:g.6443G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.263G>C	ENSP00000419905.1:p.Trp88Ser
ENST00000483553.6:c.263G>C	ENSP00000420332.2:p.Trp88Ser
ENST00000485349.6:n.304G>C
ENST00000491994.2:c.263G>C	ENSP00000417586.2:p.Trp88Ser
ENST00000494058.6:n.320G>C
ENST00000697831.1:c.263G>C	ENSP00000513453.1:p.Trp88Ser
ENST00000697832.1:n.339G>C
ENST00000697833.1:c.263G>C	ENSP00000513454.1:p.Trp88Ser
ENST00000697834.1:n.315G>C
ENST00000697835.1:c.282G>C	ENSP00000513455.1:p.Leu94=
ENST00000697836.1:n.299G>C
ENST00000697837.1:c.263G>C	ENSP00000513456.1:p.Trp88Ser
ENST00000697838.1:c.128G>C	ENSP00000513457.1:p.Trp43Ser
ENST00000697839.1:n.285G>C
ENST00000697840.1:c.263G>C	ENSP00000513458.1:p.Trp88Ser
ENST00000697841.1:n.274G>C
ENST00000697842.1:n.263G>C
ENST00000375394.7:c.263G>C MANE Select	ENSP00000364543.2:p.Trp88Ser
ENST00000375394.6:c.263G>C	ENSP00000364543.2:p.Trp88Ser
ENST00000461073.5:c.263G>C	ENSP00000419905.1:p.Trp88Ser
ENST00000465703.5:n.315G>C
ENST00000474839.5:c.127-795G>C	ENSP00000420470.1:n.127-795G>C
ENST00000488648.5:n.339G>C
ENST00000628157.1:c.127-795G>C	ENSP00000485707.1:n.127-795G>C
NM_006929.4:c.263G>C	NP_008860.4:p.Trp88Ser
XM_006715168.2:c.263G>C	XP_006715231.1:p.Trp88Ser
XM_011514815.1:c.263G>C	XP_011513117.1:p.Trp88Ser
XR_926301.1:n.351G>C
XM_011514815.3:c.263G>C	XP_011513117.1:p.Trp88Ser
XR_001743586.2:n.299G>C
XR_926301.3:n.299G>C
NM_006929.5:c.263G>C MANE Select	NP_008860.4:p.Trp88Ser