Canonical Allele Identifier: CA449812504
Gene: SKIC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31928012G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31960235G>A , CM000668.2:g.31960235G>A GRCh38
NC_000006.11:g.31928012G>A , CM000668.1:g.31928012G>A GRCh37
NC_000006.10:g.32035991G>A NCBI36
NG_032652.1:g.6432G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461073.6:c.252G>A ENSP00000419905.1:p.Lys84=
ENST00000483553.6:c.252G>A ENSP00000420332.2:p.Lys84=
ENST00000485349.6:n.293G>A
ENST00000491994.2:c.252G>A ENSP00000417586.2:p.Lys84=
ENST00000494058.6:n.309G>A
ENST00000697831.1:c.252G>A ENSP00000513453.1:p.Lys84=
ENST00000697832.1:n.328G>A
ENST00000697833.1:c.252G>A ENSP00000513454.1:p.Lys84=
ENST00000697834.1:n.304G>A
ENST00000697835.1:c.271G>A ENSP00000513455.1:p.Asp91Asn
ENST00000697836.1:n.288G>A
ENST00000697837.1:c.252G>A ENSP00000513456.1:p.Lys84=
ENST00000697838.1:c.117G>A ENSP00000513457.1:p.Lys39=
ENST00000697839.1:n.274G>A
ENST00000697840.1:c.252G>A ENSP00000513458.1:p.Lys84=
ENST00000697841.1:n.263G>A
ENST00000697842.1:n.252G>A
ENST00000375394.7:c.252G>A MANE Select ENSP00000364543.2:p.Lys84=
ENST00000375394.6:c.252G>A ENSP00000364543.2:p.Lys84=
ENST00000461073.5:c.252G>A ENSP00000419905.1:p.Lys84=
ENST00000465703.5:n.304G>A
ENST00000474839.5:c.127-806G>A ENSP00000420470.1:n.127-806G>A
ENST00000488648.5:n.328G>A
ENST00000628157.1:c.127-806G>A ENSP00000485707.1:n.127-806G>A
NM_006929.4:c.252G>A NP_008860.4:p.Lys84=
XM_006715168.2:c.252G>A XP_006715231.1:p.Lys84=
XM_011514815.1:c.252G>A XP_011513117.1:p.Lys84=
XR_926301.1:n.340G>A
XM_011514815.3:c.252G>A XP_011513117.1:p.Lys84=
XR_001743586.2:n.288G>A
XR_926301.3:n.288G>A
NM_006929.5:c.252G>A MANE Select NP_008860.4:p.Lys84=