Canonical Allele Identifier: CA1619384474

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969736A= , CM000668.2:g.31969736A=	GRCh38
NC_000006.11:g.31937513A= , CM000668.1:g.31937513A=	GRCh37
NC_000006.10:g.32045492A=	NCBI36
NG_032652.1:g.15933A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2810A=	ENSP00000419905.1:n.*2810A=
ENST00000494058.6:n.4064A=
ENST00000697831.1:c.*21A=	ENSP00000513453.1:n.*21A=
ENST00000697832.1:n.3915A=
ENST00000697835.1:c.*3280A=	ENSP00000513455.1:n.*3280A=
ENST00000697837.1:c.*878A=	ENSP00000513456.1:n.*878A=
ENST00000697838.1:c.*21A=	ENSP00000513457.1:n.*21A=
ENST00000697840.1:c.*21A=	ENSP00000513458.1:n.*21A=
ENST00000697842.1:n.4017A=
ENST00000375394.7:c.*21A= MANE Select	ENSP00000364543.2:n.*21A=
ENST00000375394.6:c.*21A=	ENSP00000364543.2:n.*21A=
ENST00000465703.5:n.4492A=
ENST00000471818.1:n.691A=
ENST00000474839.5:c.*3134A=	ENSP00000420470.1:n.*3134A=
ENST00000483553.5:c.1292A=
ENST00000491994.1:c.851A=
NM_006929.4:c.*21A=	NP_008860.4:n.*21A=
XR_926301.3:n.3778A=
NM_006929.5:c.*21A= MANE Select	NP_008860.4:n.*21A=