Canonical Allele Identifier: CA1619377079
Gene: SKIC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31959983A= , CM000668.2:g.31959983A= GRCh38
NC_000006.11:g.31927760A= , CM000668.1:g.31927760A= GRCh37
NC_000006.10:g.32035739A= NCBI36
NG_032652.1:g.6180A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461073.6:c.127-27A= ENSP00000419905.1:n.127-27A=
ENST00000483553.6:c.127-27A= ENSP00000420332.2:n.127-27A=
ENST00000485349.6:n.168-27A=
ENST00000491994.2:c.127-27A= ENSP00000417586.2:n.127-27A=
ENST00000494058.6:n.184-27A=
ENST00000697831.1:c.127-27A= ENSP00000513453.1:n.127-27A=
ENST00000697832.1:n.203-27A=
ENST00000697833.1:c.127-27A= ENSP00000513454.1:n.127-27A=
ENST00000697834.1:n.179-27A=
ENST00000697835.1:c.127-27A= ENSP00000513455.1:n.127-27A=
ENST00000697836.1:n.163-27A=
ENST00000697837.1:c.127-27A= ENSP00000513456.1:n.127-27A=
ENST00000697838.1:c.23-58A= ENSP00000513457.1:n.23-58A=
ENST00000697839.1:n.149-27A=
ENST00000697840.1:c.127-27A= ENSP00000513458.1:n.127-27A=
ENST00000697841.1:n.138-27A=
ENST00000697842.1:n.127-27A=
ENST00000375394.7:c.127-27A= MANE Select ENSP00000364543.2:n.127-27A=
ENST00000375394.6:c.127-27A= ENSP00000364543.2:n.127-27A=
ENST00000461073.5:c.127-27A= ENSP00000419905.1:n.127-27A=
ENST00000465703.5:n.179-27A=
ENST00000474839.5:c.126+583A= ENSP00000420470.1:n.126+583A=
ENST00000488648.5:n.203-27A=
ENST00000628157.1:c.126+583A= ENSP00000485707.1:n.126+583A=
NM_006929.4:c.127-27A= NP_008860.4:n.127-27A=
XM_006715168.2:c.127-27A= XP_006715231.1:n.127-27A=
XM_011514815.1:c.127-27A= XP_011513117.1:n.127-27A=
XR_926301.1:n.215-27A=
XM_011514815.3:c.127-27A= XP_011513117.1:n.127-27A=
XR_001743586.2:n.163-27A=
XR_926301.3:n.163-27A=
NM_006929.5:c.127-27A= MANE Select NP_008860.4:n.127-27A=