Canonical Allele Identifier: CA1619379142

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31962404C= , CM000668.2:g.31962404C=	GRCh38
NC_000006.11:g.31930181C= , CM000668.1:g.31930181C=	GRCh37
NC_000006.10:g.32038160C=	NCBI36
NG_032652.1:g.8601C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000461073.6:c.*181-35C=	ENSP00000419905.1:n.*181-35C=
ENST00000483553.6:c.1065-35C=	ENSP00000420332.2:n.1065-35C=
ENST00000485349.6:n.1106-35C=
ENST00000491994.2:c.1065-35C=	ENSP00000417586.2:n.1065-35C=
ENST00000494058.6:n.1122-35C=
ENST00000697831.1:c.1065-35C=	ENSP00000513453.1:n.1065-35C=
ENST00000697832.1:n.1141-35C=
ENST00000697833.1:c.1065-35C=	ENSP00000513454.1:n.1065-35C=
ENST00000697834.1:n.1117-35C=
ENST00000697835.1:c.*583-35C=	ENSP00000513455.1:n.*583-35C=
ENST00000697836.1:n.1101-35C=
ENST00000697837.1:c.1065-35C=	ENSP00000513456.1:n.1065-35C=
ENST00000697838.1:c.930-35C=	ENSP00000513457.1:n.930-35C=
ENST00000697839.1:n.1348-35C=
ENST00000697840.1:c.1101-35C=	ENSP00000513458.1:n.1101-35C=
ENST00000697841.1:n.1637-35C=
ENST00000697842.1:n.1065-35C=
ENST00000375394.7:c.1065-35C= MANE Select	ENSP00000364543.2:n.1065-35C=
ENST00000375394.6:c.1065-35C=	ENSP00000364543.2:n.1065-35C=
ENST00000461073.5:c.*181-35C=	ENSP00000419905.1:n.*181-35C=
ENST00000465703.5:n.1378-35C=
ENST00000466290.1:n.326-35C=
ENST00000474839.5:c.*437-35C=	ENSP00000420470.1:n.*437-35C=
NM_006929.4:c.1065-35C=	NP_008860.4:n.1065-35C=
XM_006715168.2:c.1065-35C=	XP_006715231.1:n.1065-35C=
XM_011514815.1:c.1065-35C=	XP_011513117.1:n.1065-35C=
XR_926301.1:n.1153-35C=
XM_011514815.3:c.1065-35C=	XP_011513117.1:n.1065-35C=
XR_001743586.2:n.1101-35C=
XR_926301.3:n.1101-35C=
NM_006929.5:c.1065-35C= MANE Select	NP_008860.4:n.1065-35C=