Canonical Allele Identifier: CA136914595

Gene: SKIC2

Linked Data

• dbSNP Id: rs913096735
• MyVariant Identifiers: chr6:g.31937277C>G (hg19) ; chr6:g.31969500C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969500C>G , CM000668.2:g.31969500C>G	GRCh38
NC_000006.11:g.31937277C>G , CM000668.1:g.31937277C>G	GRCh37
NC_000006.10:g.32045256C>G	NCBI36
NG_032652.1:g.15697C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2574C>G	ENSP00000419905.1:n.*2574C>G
ENST00000483553.6:c.*587C>G	ENSP00000420332.2:n.*587C>G
ENST00000485349.6:n.4017-15C>G
ENST00000491994.2:c.*68C>G	ENSP00000417586.2:n.*68C>G
ENST00000494058.6:n.3843-15C>G
ENST00000697831.1:c.3472-15C>G	ENSP00000513453.1:n.3472-15C>G
ENST00000697832.1:n.3694-15C>G
ENST00000697833.1:c.*489-15C>G	ENSP00000513454.1:n.*489-15C>G
ENST00000697834.1:n.4244C>G
ENST00000697835.1:c.*3059-15C>G	ENSP00000513455.1:n.*3059-15C>G
ENST00000697836.1:n.3880C>G
ENST00000697837.1:c.*657-15C>G	ENSP00000513456.1:n.*657-15C>G
ENST00000697838.1:c.3406-15C>G	ENSP00000513457.1:n.3406-15C>G
ENST00000697839.1:n.4338C>G
ENST00000697840.1:c.3577-15C>G	ENSP00000513458.1:n.3577-15C>G
ENST00000697841.1:n.4437C>G
ENST00000697842.1:n.3796-15C>G
ENST00000375394.7:c.3541-15C>G MANE Select	ENSP00000364543.2:n.3541-15C>G
ENST00000375394.6:c.3541-15C>G	ENSP00000364543.2:n.3541-15C>G
ENST00000465703.5:n.4256C>G
ENST00000470453.1:n.383-15C>G
ENST00000471818.1:n.470-15C>G
ENST00000474839.5:c.*2913-15C>G	ENSP00000420470.1:n.*2913-15C>G
ENST00000483553.5:c.1056C>G
ENST00000491994.1:c.615C>G
NM_006929.4:c.3541-15C>G	NP_008860.4:n.3541-15C>G
XR_001743586.2:n.3719C>G
XR_926301.3:n.3557-15C>G
NM_006929.5:c.3541-15C>G MANE Select	NP_008860.4:n.3541-15C>G