Canonical Allele Identifier: CA1619379228
Gene: SKIC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31962497A= , CM000668.2:g.31962497A= GRCh38
NC_000006.11:g.31930274A= , CM000668.1:g.31930274A= GRCh37
NC_000006.10:g.32038253A= NCBI36
NG_032652.1:g.8694A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461073.6:c.*239A= ENSP00000419905.1:n.*239A=
ENST00000483553.6:c.1123A= ENSP00000420332.2:p.Asn375=
ENST00000485349.6:n.1164A=
ENST00000491994.2:c.1123A= ENSP00000417586.2:p.Asn375=
ENST00000494058.6:n.1180A=
ENST00000697831.1:c.1123A= ENSP00000513453.1:p.Asn375=
ENST00000697832.1:n.1199A=
ENST00000697833.1:c.1123A= ENSP00000513454.1:p.Asn375=
ENST00000697834.1:n.1175A=
ENST00000697835.1:c.*641A= ENSP00000513455.1:n.*641A=
ENST00000697836.1:n.1159A=
ENST00000697837.1:c.1123A= ENSP00000513456.1:p.Asn375=
ENST00000697838.1:c.988A= ENSP00000513457.1:p.Asn330=
ENST00000697839.1:n.1406A=
ENST00000697840.1:c.1159A= ENSP00000513458.1:p.Asn387=
ENST00000697841.1:n.1695A=
ENST00000697842.1:n.1123A=
ENST00000375394.7:c.1123A= MANE Select ENSP00000364543.2:p.Asn375=
ENST00000375394.6:c.1123A= ENSP00000364543.2:p.Asn375=
ENST00000461073.5:c.*239A= ENSP00000419905.1:n.*239A=
ENST00000465703.5:n.1436A=
ENST00000466290.1:n.384A=
ENST00000474839.5:c.*495A= ENSP00000420470.1:n.*495A=
NM_006929.4:c.1123A= NP_008860.4:p.Asn375=
XM_006715168.2:c.1123A= XP_006715231.1:p.Asn375=
XM_011514815.1:c.1123A= XP_011513117.1:p.Asn375=
XR_926301.1:n.1211A=
XM_011514815.3:c.1123A= XP_011513117.1:p.Asn375=
XR_001743586.2:n.1159A=
XR_926301.3:n.1159A=
NM_006929.5:c.1123A= MANE Select NP_008860.4:p.Asn375=