Canonical Allele Identifier: CA2711460134

Gene: SKIC2

Linked Data

• dbSNP Id: rs2151818367

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969732C>T , CM000668.2:g.31969732C>T	GRCh38
NC_000006.11:g.31937509C>T , CM000668.1:g.31937509C>T	GRCh37
NC_000006.10:g.32045488C>T	NCBI36
NG_032652.1:g.15929C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2806C>T	ENSP00000419905.1:n.*2806C>T
ENST00000494058.6:n.4060C>T
ENST00000697831.1:c.*17C>T	ENSP00000513453.1:n.*17C>T
ENST00000697832.1:n.3911C>T
ENST00000697835.1:c.*3276C>T	ENSP00000513455.1:n.*3276C>T
ENST00000697837.1:c.*874C>T	ENSP00000513456.1:n.*874C>T
ENST00000697838.1:c.*17C>T	ENSP00000513457.1:n.*17C>T
ENST00000697840.1:c.*17C>T	ENSP00000513458.1:n.*17C>T
ENST00000697842.1:n.4013C>T
ENST00000375394.7:c.*17C>T MANE Select	ENSP00000364543.2:n.*17C>T
ENST00000375394.6:c.*17C>T	ENSP00000364543.2:n.*17C>T
ENST00000465703.5:n.4488C>T
ENST00000471818.1:n.687C>T
ENST00000474839.5:c.*3130C>T	ENSP00000420470.1:n.*3130C>T
ENST00000483553.5:c.1288C>T
ENST00000491994.1:c.847C>T
NM_006929.4:c.*17C>T	NP_008860.4:n.*17C>T
XR_926301.3:n.3774C>T
NM_006929.5:c.*17C>T MANE Select	NP_008860.4:n.*17C>T