Canonical Allele Identifier: CA363492607

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937484A>T (hg19) ; chr6:g.31969707A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969707A>T , CM000668.2:g.31969707A>T	GRCh38
NC_000006.11:g.31937484A>T , CM000668.1:g.31937484A>T	GRCh37
NC_000006.10:g.32045463A>T	NCBI36
NG_032652.1:g.15904A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2781A>T	ENSP00000419905.1:n.*2781A>T
ENST00000485349.6:n.4209A>T
ENST00000491994.2:c.*275A>T	ENSP00000417586.2:n.*275A>T
ENST00000494058.6:n.4035A>T
ENST00000697831.1:c.3664A>T	ENSP00000513453.1:p.Thr1222Ser
ENST00000697832.1:n.3886A>T
ENST00000697834.1:n.4451A>T
ENST00000697835.1:c.*3251A>T	ENSP00000513455.1:n.*3251A>T
ENST00000697837.1:c.*849A>T	ENSP00000513456.1:n.*849A>T
ENST00000697838.1:c.3598A>T	ENSP00000513457.1:p.Thr1200Ser
ENST00000697839.1:n.4545A>T
ENST00000697840.1:c.3769A>T	ENSP00000513458.1:p.Thr1257Ser
ENST00000697841.1:n.4644A>T
ENST00000697842.1:n.3988A>T
ENST00000375394.7:c.3733A>T MANE Select	ENSP00000364543.2:p.Thr1245Ser
ENST00000375394.6:c.3733A>T	ENSP00000364543.2:p.Thr1245Ser
ENST00000465703.5:n.4463A>T
ENST00000471818.1:n.662A>T
ENST00000474839.5:c.*3105A>T	ENSP00000420470.1:n.*3105A>T
ENST00000483553.5:c.1263A>T
ENST00000491994.1:c.822A>T
NM_006929.4:c.3733A>T	NP_008860.4:p.Thr1245Ser
XR_926301.3:n.3749A>T
NM_006929.5:c.3733A>T MANE Select	NP_008860.4:p.Thr1245Ser