Canonical Allele Identifier: CA1099601399
Gene: SKAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26852010_26852011insGT , CM000669.2:g.26852010_26852011insGT GRCh38
NC_000007.13:g.26891629_26891630insGT , CM000669.1:g.26891629_26891630insGT GRCh37
NC_000007.12:g.26858154_26858155insGT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000345317.7:c.199+2126_199+2127insAC MANE Select ENSP00000005587.2:n.199+2126_199+2127insA...
ENST00000345317.6:c.199+2126_199+2127insAC ENSP00000005587.2:n.199+2126_199+2127insA...
ENST00000432747.1:c.154+2126_154+2127insAC ENSP00000408163.1:n.154+2126_154+2127insA...
ENST00000468712.5:n.360+2126_360+2127insAC
ENST00000481204.5:n.404+2126_404+2127insAC
ENST00000487720.1:n.355+2126_355+2127insAC
ENST00000490456.6:n.372+2126_372+2127insAC
ENST00000495802.5:n.166+2126_166+2127insAC
ENST00000497511.5:n.357+2126_357+2127insAC
NM_001303468.1:c.-318+2126_-318+2127insAC NP_001290397.1:n.-318+2126_-318+2127insAC...
NM_003930.4:c.199+2126_199+2127insAC NP_003921.2:n.199+2126_199+2127insAC
XR_927132.1:n.252-5454_252-5453insGT
XM_017012771.2:c.199+2126_199+2127insAC XP_016868260.1:n.199+2126_199+2127insAC
NM_003930.5:c.199+2126_199+2127insAC MANE Select NP_003921.2:n.199+2126_199+2127insAC
NM_001303468.2:c.-318+2126_-318+2127insAC NP_001290397.1:n.-318+2126_-318+2127insAC...