Canonical Allele Identifier: CA1619384473

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969734T= , CM000668.2:g.31969734T=	GRCh38
NC_000006.11:g.31937511T= , CM000668.1:g.31937511T=	GRCh37
NC_000006.10:g.32045490T=	NCBI36
NG_032652.1:g.15931T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2808T=	ENSP00000419905.1:n.*2808T=
ENST00000494058.6:n.4062T=
ENST00000697831.1:c.*19T=	ENSP00000513453.1:n.*19T=
ENST00000697832.1:n.3913T=
ENST00000697835.1:c.*3278T=	ENSP00000513455.1:n.*3278T=
ENST00000697837.1:c.*876T=	ENSP00000513456.1:n.*876T=
ENST00000697838.1:c.*19T=	ENSP00000513457.1:n.*19T=
ENST00000697840.1:c.*19T=	ENSP00000513458.1:n.*19T=
ENST00000697842.1:n.4015T=
ENST00000375394.7:c.*19T= MANE Select	ENSP00000364543.2:n.*19T=
ENST00000375394.6:c.*19T=	ENSP00000364543.2:n.*19T=
ENST00000465703.5:n.4490T=
ENST00000471818.1:n.689T=
ENST00000474839.5:c.*3132T=	ENSP00000420470.1:n.*3132T=
ENST00000483553.5:c.1290T=
ENST00000491994.1:c.849T=
NM_006929.4:c.*19T=	NP_008860.4:n.*19T=
XR_926301.3:n.3776T=
NM_006929.5:c.*19T= MANE Select	NP_008860.4:n.*19T=