Canonical Allele Identifier: CA2678079024

Gene: SKIC2

Linked Data

• gnomAD v4: 6-31969724-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969725del , CM000668.2:g.31969725del	GRCh38
NC_000006.11:g.31937502del , CM000668.1:g.31937502del	GRCh37
NC_000006.10:g.32045481del	NCBI36
NG_032652.1:g.15922del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2799del	ENSP00000419905.1:n.*2799del
ENST00000494058.6:n.4053del
ENST00000697831.1:c.*10del	ENSP00000513453.1:n.*10del
ENST00000697832.1:n.3904del
ENST00000697835.1:c.*3269del	ENSP00000513455.1:n.*3269del
ENST00000697837.1:c.*867del	ENSP00000513456.1:n.*867del
ENST00000697838.1:c.*10del	ENSP00000513457.1:n.*10del
ENST00000697840.1:c.*10del	ENSP00000513458.1:n.*10del
ENST00000697841.1:n.4662del
ENST00000697842.1:n.4006del
ENST00000375394.7:c.*10del MANE Select	ENSP00000364543.2:n.*10del
ENST00000375394.6:c.*10del	ENSP00000364543.2:n.*10del
ENST00000465703.5:n.4481del
ENST00000471818.1:n.680del
ENST00000474839.5:c.*3123del	ENSP00000420470.1:n.*3123del
ENST00000483553.5:c.1281del
ENST00000491994.1:c.840del
NM_006929.4:c.*10del	NP_008860.4:n.*10del
XR_926301.3:n.3767del
NM_006929.5:c.*10del MANE Select	NP_008860.4:n.*10del