Canonical Allele Identifier: CA449813932

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937194C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969417C>A , CM000668.2:g.31969417C>A	GRCh38
NC_000006.11:g.31937194C>A , CM000668.1:g.31937194C>A	GRCh37
NC_000006.10:g.32045173C>A	NCBI36
NG_032652.1:g.15614C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2491C>A	ENSP00000419905.1:n.*2491C>A
ENST00000483553.6:c.*504C>A	ENSP00000420332.2:n.*504C>A
ENST00000485349.6:n.4013C>A
ENST00000491994.2:c.3537C>A	ENSP00000417586.2:p.Gly1179=
ENST00000494058.6:n.3839C>A
ENST00000697831.1:c.3468C>A	ENSP00000513453.1:p.Gly1156=
ENST00000697832.1:n.3690C>A
ENST00000697833.1:c.*485C>A	ENSP00000513454.1:n.*485C>A
ENST00000697834.1:n.4161C>A
ENST00000697835.1:c.*3055C>A	ENSP00000513455.1:n.*3055C>A
ENST00000697836.1:n.3868C>A
ENST00000697837.1:c.*653C>A	ENSP00000513456.1:n.*653C>A
ENST00000697838.1:c.3402C>A	ENSP00000513457.1:p.Gly1134=
ENST00000697839.1:n.4255C>A
ENST00000697840.1:c.3573C>A	ENSP00000513458.1:p.Gly1191=
ENST00000697841.1:n.4354C>A
ENST00000697842.1:n.3792C>A
ENST00000375394.7:c.3537C>A MANE Select	ENSP00000364543.2:p.Gly1179=
ENST00000375394.6:c.3537C>A	ENSP00000364543.2:p.Gly1179=
ENST00000465703.5:n.4173C>A
ENST00000470453.1:n.383-98C>A
ENST00000471818.1:n.466C>A
ENST00000474839.5:c.*2909C>A	ENSP00000420470.1:n.*2909C>A
ENST00000483553.5:c.973C>A
ENST00000491994.1:c.532C>A
NM_006929.4:c.3537C>A	NP_008860.4:p.Gly1179=
XR_001743586.2:n.3636C>A
XR_926301.3:n.3553C>A
NM_006929.5:c.3537C>A MANE Select	NP_008860.4:p.Gly1179=