Canonical Allele Identifier: CA1619384469

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969727A= , CM000668.2:g.31969727A=	GRCh38
NC_000006.11:g.31937504A= , CM000668.1:g.31937504A=	GRCh37
NC_000006.10:g.32045483A=	NCBI36
NG_032652.1:g.15924A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2801A=	ENSP00000419905.1:n.*2801A=
ENST00000494058.6:n.4055A=
ENST00000697831.1:c.*12A=	ENSP00000513453.1:n.*12A=
ENST00000697832.1:n.3906A=
ENST00000697835.1:c.*3271A=	ENSP00000513455.1:n.*3271A=
ENST00000697837.1:c.*869A=	ENSP00000513456.1:n.*869A=
ENST00000697838.1:c.*12A=	ENSP00000513457.1:n.*12A=
ENST00000697840.1:c.*12A=	ENSP00000513458.1:n.*12A=
ENST00000697841.1:n.4664A=
ENST00000697842.1:n.4008A=
ENST00000375394.7:c.*12A= MANE Select	ENSP00000364543.2:n.*12A=
ENST00000375394.6:c.*12A=	ENSP00000364543.2:n.*12A=
ENST00000465703.5:n.4483A=
ENST00000471818.1:n.682A=
ENST00000474839.5:c.*3125A=	ENSP00000420470.1:n.*3125A=
ENST00000483553.5:c.1283A=
ENST00000491994.1:c.842A=
NM_006929.4:c.*12A=	NP_008860.4:n.*12A=
XR_926301.3:n.3769A=
NM_006929.5:c.*12A= MANE Select	NP_008860.4:n.*12A=