Canonical Allele Identifier: CA449814178

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937411T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969634T>A , CM000668.2:g.31969634T>A	GRCh38
NC_000006.11:g.31937411T>A , CM000668.1:g.31937411T>A	GRCh37
NC_000006.10:g.32045390T>A	NCBI36
NG_032652.1:g.15831T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2708T>A	ENSP00000419905.1:n.*2708T>A
ENST00000485349.6:n.4136T>A
ENST00000491994.2:c.*202T>A	ENSP00000417586.2:n.*202T>A
ENST00000494058.6:n.3962T>A
ENST00000697831.1:c.3591T>A	ENSP00000513453.1:p.Pro1197=
ENST00000697832.1:n.3813T>A
ENST00000697834.1:n.4378T>A
ENST00000697835.1:c.*3178T>A	ENSP00000513455.1:n.*3178T>A
ENST00000697836.1:n.4014T>A
ENST00000697837.1:c.*776T>A	ENSP00000513456.1:n.*776T>A
ENST00000697838.1:c.3525T>A	ENSP00000513457.1:p.Pro1175=
ENST00000697839.1:n.4472T>A
ENST00000697840.1:c.3696T>A	ENSP00000513458.1:p.Pro1232=
ENST00000697841.1:n.4571T>A
ENST00000697842.1:n.3915T>A
ENST00000375394.7:c.3660T>A MANE Select	ENSP00000364543.2:p.Pro1220=
ENST00000375394.6:c.3660T>A	ENSP00000364543.2:p.Pro1220=
ENST00000465703.5:n.4390T>A
ENST00000471818.1:n.589T>A
ENST00000474839.5:c.*3032T>A	ENSP00000420470.1:n.*3032T>A
ENST00000483553.5:c.1190T>A
ENST00000491994.1:c.749T>A
NM_006929.4:c.3660T>A	NP_008860.4:p.Pro1220=
XR_926301.3:n.3676T>A
NM_006929.5:c.3660T>A MANE Select	NP_008860.4:p.Pro1220=