Canonical Allele Identifier: CA2678078829

Gene: SKIC2

Linked Data

• gnomAD v4: 6-31969437-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969437T>C , CM000668.2:g.31969437T>C	GRCh38
NC_000006.11:g.31937214T>C , CM000668.1:g.31937214T>C	GRCh37
NC_000006.10:g.32045193T>C	NCBI36
NG_032652.1:g.15634T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2511T>C	ENSP00000419905.1:n.*2511T>C
ENST00000483553.6:c.*524T>C	ENSP00000420332.2:n.*524T>C
ENST00000485349.6:n.4016+17T>C
ENST00000491994.2:c.*5T>C	ENSP00000417586.2:n.*5T>C
ENST00000494058.6:n.3842+17T>C
ENST00000697831.1:c.3471+17T>C	ENSP00000513453.1:n.3471+17T>C
ENST00000697832.1:n.3693+17T>C
ENST00000697833.1:c.*488+17T>C	ENSP00000513454.1:n.*488+17T>C
ENST00000697834.1:n.4181T>C
ENST00000697835.1:c.*3058+17T>C	ENSP00000513455.1:n.*3058+17T>C
ENST00000697836.1:n.3871+17T>C
ENST00000697837.1:c.*656+17T>C	ENSP00000513456.1:n.*656+17T>C
ENST00000697838.1:c.3405+17T>C	ENSP00000513457.1:n.3405+17T>C
ENST00000697839.1:n.4275T>C
ENST00000697840.1:c.3576+17T>C	ENSP00000513458.1:n.3576+17T>C
ENST00000697841.1:n.4374T>C
ENST00000697842.1:n.3795+17T>C
ENST00000375394.7:c.3540+17T>C MANE Select	ENSP00000364543.2:n.3540+17T>C
ENST00000375394.6:c.3540+17T>C	ENSP00000364543.2:n.3540+17T>C
ENST00000465703.5:n.4193T>C
ENST00000470453.1:n.383-78T>C
ENST00000471818.1:n.469+17T>C
ENST00000474839.5:c.*2912+17T>C	ENSP00000420470.1:n.*2912+17T>C
ENST00000483553.5:c.993T>C
ENST00000491994.1:c.552T>C
NM_006929.4:c.3540+17T>C	NP_008860.4:n.3540+17T>C
XR_001743586.2:n.3656T>C
XR_926301.3:n.3556+17T>C
NM_006929.5:c.3540+17T>C MANE Select	NP_008860.4:n.3540+17T>C