Canonical Allele Identifier: CA1619384471

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969732_31969735delinsCATG , CM000668.2:g.31969732_31969735delinsCATG	GRCh38
NC_000006.11:g.31937509_31937512delinsCATG , CM000668.1:g.31937509_31937512delinsCATG	GRCh37
NC_000006.10:g.32045488_32045491delinsCATG	NCBI36
NG_032652.1:g.15929_15932delinsCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2806_*2809delinsCATG	ENSP00000419905.1:n.*2806_*2809delinsCATG
ENST00000494058.6:n.4060_4063delinsCATG
ENST00000697831.1:c.*17_*20delinsCATG	ENSP00000513453.1:n.*17_*20delinsCATG
ENST00000697832.1:n.3911_3914delinsCATG
ENST00000697835.1:c.*3276_*3279delinsCATG	ENSP00000513455.1:n.*3276_*3279delinsCATG
ENST00000697837.1:c.*874_*877delinsCATG	ENSP00000513456.1:n.*874_*877delinsCATG
ENST00000697838.1:c.*17_*20delinsCATG	ENSP00000513457.1:n.*17_*20delinsCATG
ENST00000697840.1:c.*17_*20delinsCATG	ENSP00000513458.1:n.*17_*20delinsCATG
ENST00000697842.1:n.4013_4016delinsCATG
ENST00000375394.7:c.*17_*20delinsCATG MANE Select	ENSP00000364543.2:n.*17_*20delinsCATG
ENST00000375394.6:c.*17_*20delinsCATG	ENSP00000364543.2:n.*17_*20delinsCATG
ENST00000465703.5:n.4488_4491delinsCATG
ENST00000471818.1:n.687_690delinsCATG
ENST00000474839.5:c.*3130_*3133delinsCATG	ENSP00000420470.1:n.*3130_*3133delinsCATG
ENST00000483553.5:c.1288_1291delinsCATG
ENST00000491994.1:c.847_850delinsCATG
NM_006929.4:c.*17_*20delinsCATG	NP_008860.4:n.*17_*20delinsCATG
XR_926301.3:n.3774_3777delinsCATG
NM_006929.5:c.*17_*20delinsCATG MANE Select	NP_008860.4:n.*17_*20delinsCATG