Canonical Allele Identifier: CA363434557

Gene: SKIC2

Linked Data

• gnomAD v4: 6-31960073-T-A
• MyVariant Identifiers: chr6:g.31927850T>A (hg19) ; chr6:g.31960073T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960073T>A , CM000668.2:g.31960073T>A	GRCh38
NC_000006.11:g.31927850T>A , CM000668.1:g.31927850T>A	GRCh37
NC_000006.10:g.32035829T>A	NCBI36
NG_032652.1:g.6270T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.190T>A	ENSP00000419905.1:p.Ser64Thr
ENST00000483553.6:c.190T>A	ENSP00000420332.2:p.Ser64Thr
ENST00000485349.6:n.231T>A
ENST00000491994.2:c.190T>A	ENSP00000417586.2:p.Ser64Thr
ENST00000494058.6:n.247T>A
ENST00000697831.1:c.190T>A	ENSP00000513453.1:p.Ser64Thr
ENST00000697832.1:n.266T>A
ENST00000697833.1:c.190T>A	ENSP00000513454.1:p.Ser64Thr
ENST00000697834.1:n.242T>A
ENST00000697835.1:c.190T>A	ENSP00000513455.1:p.Ser64Thr
ENST00000697836.1:n.226T>A
ENST00000697837.1:c.190T>A	ENSP00000513456.1:p.Ser64Thr
ENST00000697838.1:c.55T>A	ENSP00000513457.1:p.Ser19Thr
ENST00000697839.1:n.212T>A
ENST00000697840.1:c.190T>A	ENSP00000513458.1:p.Ser64Thr
ENST00000697841.1:n.201T>A
ENST00000697842.1:n.190T>A
ENST00000375394.7:c.190T>A MANE Select	ENSP00000364543.2:p.Ser64Thr
ENST00000375394.6:c.190T>A	ENSP00000364543.2:p.Ser64Thr
ENST00000461073.5:c.190T>A	ENSP00000419905.1:p.Ser64Thr
ENST00000465703.5:n.242T>A
ENST00000474839.5:c.126+673T>A	ENSP00000420470.1:n.126+673T>A
ENST00000488648.5:n.266T>A
ENST00000628157.1:c.126+673T>A	ENSP00000485707.1:n.126+673T>A
NM_006929.4:c.190T>A	NP_008860.4:p.Ser64Thr
XM_006715168.2:c.190T>A	XP_006715231.1:p.Ser64Thr
XM_011514815.1:c.190T>A	XP_011513117.1:p.Ser64Thr
XR_926301.1:n.278T>A
XM_011514815.3:c.190T>A	XP_011513117.1:p.Ser64Thr
XR_001743586.2:n.226T>A
XR_926301.3:n.226T>A
NM_006929.5:c.190T>A MANE Select	NP_008860.4:p.Ser64Thr