Canonical Allele Identifier: CA363450915

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31930277A>T (hg19) ; chr6:g.31962500A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31962500A>T , CM000668.2:g.31962500A>T	GRCh38
NC_000006.11:g.31930277A>T , CM000668.1:g.31930277A>T	GRCh37
NC_000006.10:g.32038256A>T	NCBI36
NG_032652.1:g.8697A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*242A>T	ENSP00000419905.1:n.*242A>T
ENST00000483553.6:c.1126A>T	ENSP00000420332.2:p.Thr376Ser
ENST00000485349.6:n.1167A>T
ENST00000491994.2:c.1126A>T	ENSP00000417586.2:p.Thr376Ser
ENST00000494058.6:n.1183A>T
ENST00000697831.1:c.1126A>T	ENSP00000513453.1:p.Thr376Ser
ENST00000697832.1:n.1202A>T
ENST00000697833.1:c.1126A>T	ENSP00000513454.1:p.Thr376Ser
ENST00000697834.1:n.1178A>T
ENST00000697835.1:c.*644A>T	ENSP00000513455.1:n.*644A>T
ENST00000697836.1:n.1162A>T
ENST00000697837.1:c.1126A>T	ENSP00000513456.1:p.Thr376Ser
ENST00000697838.1:c.991A>T	ENSP00000513457.1:p.Thr331Ser
ENST00000697839.1:n.1409A>T
ENST00000697840.1:c.1162A>T	ENSP00000513458.1:p.Thr388Ser
ENST00000697841.1:n.1698A>T
ENST00000697842.1:n.1126A>T
ENST00000375394.7:c.1126A>T MANE Select	ENSP00000364543.2:p.Thr376Ser
ENST00000375394.6:c.1126A>T	ENSP00000364543.2:p.Thr376Ser
ENST00000461073.5:c.*242A>T	ENSP00000419905.1:n.*242A>T
ENST00000465703.5:n.1439A>T
ENST00000466290.1:n.387A>T
ENST00000474839.5:c.*498A>T	ENSP00000420470.1:n.*498A>T
NM_006929.4:c.1126A>T	NP_008860.4:p.Thr376Ser
XM_006715168.2:c.1126A>T	XP_006715231.1:p.Thr376Ser
XM_011514815.1:c.1126A>T	XP_011513117.1:p.Thr376Ser
XR_926301.1:n.1214A>T
XM_011514815.3:c.1126A>T	XP_011513117.1:p.Thr376Ser
XR_001743586.2:n.1162A>T
XR_926301.3:n.1162A>T
NM_006929.5:c.1126A>T MANE Select	NP_008860.4:p.Thr376Ser