Canonical Allele Identifier: CA449814233

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937459C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969682C>T , CM000668.2:g.31969682C>T	GRCh38
NC_000006.11:g.31937459C>T , CM000668.1:g.31937459C>T	GRCh37
NC_000006.10:g.32045438C>T	NCBI36
NG_032652.1:g.15879C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2756C>T	ENSP00000419905.1:n.*2756C>T
ENST00000485349.6:n.4184C>T
ENST00000491994.2:c.*250C>T	ENSP00000417586.2:n.*250C>T
ENST00000494058.6:n.4010C>T
ENST00000697831.1:c.3639C>T	ENSP00000513453.1:p.Asp1213=
ENST00000697832.1:n.3861C>T
ENST00000697834.1:n.4426C>T
ENST00000697835.1:c.*3226C>T	ENSP00000513455.1:n.*3226C>T
ENST00000697836.1:n.4062C>T
ENST00000697837.1:c.*824C>T	ENSP00000513456.1:n.*824C>T
ENST00000697838.1:c.3573C>T	ENSP00000513457.1:p.Asp1191=
ENST00000697839.1:n.4520C>T
ENST00000697840.1:c.3744C>T	ENSP00000513458.1:p.Asp1248=
ENST00000697841.1:n.4619C>T
ENST00000697842.1:n.3963C>T
ENST00000375394.7:c.3708C>T MANE Select	ENSP00000364543.2:p.Asp1236=
ENST00000375394.6:c.3708C>T	ENSP00000364543.2:p.Asp1236=
ENST00000465703.5:n.4438C>T
ENST00000471818.1:n.637C>T
ENST00000474839.5:c.*3080C>T	ENSP00000420470.1:n.*3080C>T
ENST00000483553.5:c.1238C>T
ENST00000491994.1:c.797C>T
NM_006929.4:c.3708C>T	NP_008860.4:p.Asp1236=
XR_926301.3:n.3724C>T
NM_006929.5:c.3708C>T MANE Select	NP_008860.4:p.Asp1236=