Canonical Allele Identifier: CA2842836943

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969722dup , CM000668.2:g.31969722dup	GRCh38
NC_000006.11:g.31937499dup , CM000668.1:g.31937499dup	GRCh37
NC_000006.10:g.32045478dup	NCBI36
NG_032652.1:g.15919dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2796dup	ENSP00000419905.1:n.*2796dup
ENST00000494058.6:n.4050dup
ENST00000697831.1:c.*7dup	ENSP00000513453.1:n.*7dup
ENST00000697832.1:n.3901dup
ENST00000697835.1:c.*3266dup	ENSP00000513455.1:n.*3266dup
ENST00000697837.1:c.*864dup	ENSP00000513456.1:n.*864dup
ENST00000697838.1:c.*7dup	ENSP00000513457.1:n.*7dup
ENST00000697839.1:n.4560dup
ENST00000697840.1:c.*7dup	ENSP00000513458.1:n.*7dup
ENST00000697841.1:n.4659dup
ENST00000697842.1:n.4003dup
ENST00000375394.7:c.*7dup MANE Select	ENSP00000364543.2:n.*7dup
ENST00000375394.6:c.*7dup	ENSP00000364543.2:n.*7dup
ENST00000465703.5:n.4478dup
ENST00000471818.1:n.677dup
ENST00000474839.5:c.*3120dup	ENSP00000420470.1:n.*3120dup
ENST00000483553.5:c.1278dup
ENST00000491994.1:c.837dup
NM_006929.4:c.*7dup	NP_008860.4:n.*7dup
XR_926301.3:n.3764dup
NM_006929.5:c.*7dup MANE Select	NP_008860.4:n.*7dup