Canonical Allele Identifier: CA1696086303
Gene: SKAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.26852045A= , CM000669.2:g.26852045A= GRCh38
NC_000007.13:g.26891664A= , CM000669.1:g.26891664A= GRCh37
NC_000007.12:g.26858189A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000345317.7:c.199+2092T= MANE Select ENSP00000005587.2:n.199+2092T=
ENST00000345317.6:c.199+2092T= ENSP00000005587.2:n.199+2092T=
ENST00000432747.1:c.154+2092T= ENSP00000408163.1:n.154+2092T=
ENST00000468712.5:n.360+2092T=
ENST00000481204.5:n.404+2092T=
ENST00000487720.1:n.355+2092T=
ENST00000490456.6:n.372+2092T=
ENST00000495802.5:n.166+2092T=
ENST00000497511.5:n.357+2092T=
NM_001303468.1:c.-318+2092T= NP_001290397.1:n.-318+2092T=
NM_003930.4:c.199+2092T= NP_003921.2:n.199+2092T=
XR_927132.1:n.252-5419A=
XM_017012771.2:c.199+2092T= XP_016868260.1:n.199+2092T=
NM_003930.5:c.199+2092T= MANE Select NP_003921.2:n.199+2092T=
NM_001303468.2:c.-318+2092T= NP_001290397.1:n.-318+2092T=