Canonical Allele Identifier: CA449814061

Gene: SKIC2

Linked Data

• MyVariant Identifiers: chr6:g.31937309A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969532A>T , CM000668.2:g.31969532A>T	GRCh38
NC_000006.11:g.31937309A>T , CM000668.1:g.31937309A>T	GRCh37
NC_000006.10:g.32045288A>T	NCBI36
NG_032652.1:g.15729A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2606A>T	ENSP00000419905.1:n.*2606A>T
ENST00000485349.6:n.4034A>T
ENST00000491994.2:c.*100A>T	ENSP00000417586.2:n.*100A>T
ENST00000494058.6:n.3860A>T
ENST00000697831.1:c.3489A>T	ENSP00000513453.1:p.Ala1163=
ENST00000697832.1:n.3711A>T
ENST00000697833.1:c.*506A>T	ENSP00000513454.1:n.*506A>T
ENST00000697834.1:n.4276A>T
ENST00000697835.1:c.*3076A>T	ENSP00000513455.1:n.*3076A>T
ENST00000697836.1:n.3912A>T
ENST00000697837.1:c.*674A>T	ENSP00000513456.1:n.*674A>T
ENST00000697838.1:c.3423A>T	ENSP00000513457.1:p.Ala1141=
ENST00000697839.1:n.4370A>T
ENST00000697840.1:c.3594A>T	ENSP00000513458.1:p.Ala1198=
ENST00000697841.1:n.4469A>T
ENST00000697842.1:n.3813A>T
ENST00000375394.7:c.3558A>T MANE Select	ENSP00000364543.2:p.Ala1186=
ENST00000375394.6:c.3558A>T	ENSP00000364543.2:p.Ala1186=
ENST00000465703.5:n.4288A>T
ENST00000470453.1:n.400A>T
ENST00000471818.1:n.487A>T
ENST00000474839.5:c.*2930A>T	ENSP00000420470.1:n.*2930A>T
ENST00000483553.5:c.1088A>T
ENST00000491994.1:c.647A>T
NM_006929.4:c.3558A>T	NP_008860.4:p.Ala1186=
XR_926301.3:n.3574A>T
NM_006929.5:c.3558A>T MANE Select	NP_008860.4:p.Ala1186=