Canonical Allele Identifier: CA1099601456

Gene: SKAP2

Linked Data

• dbSNP Id: rs1785054955
• gnomAD v3: 7-26852030-AGGAG-A
• gnomAD v4: 7-26852030-AGGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.26852032_26852035del , CM000669.2:g.26852032_26852035del	GRCh38
NC_000007.13:g.26891651_26891654del , CM000669.1:g.26891651_26891654del	GRCh37
NC_000007.12:g.26858176_26858179del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345317.7:c.199+2103_199+2106del MANE Select	ENSP00000005587.2:n.199+2103_199+2106del
ENST00000345317.6:c.199+2103_199+2106del	ENSP00000005587.2:n.199+2103_199+2106del
ENST00000432747.1:c.154+2103_154+2106del	ENSP00000408163.1:n.154+2103_154+2106del
ENST00000468712.5:n.360+2103_360+2106del
ENST00000481204.5:n.404+2103_404+2106del
ENST00000487720.1:n.355+2103_355+2106del
ENST00000490456.6:n.372+2103_372+2106del
ENST00000495802.5:n.166+2103_166+2106del
ENST00000497511.5:n.357+2103_357+2106del
NM_001303468.1:c.-318+2103_-318+2106del	NP_001290397.1:n.-318+2103_-318+2106del
NM_003930.4:c.199+2103_199+2106del	NP_003921.2:n.199+2103_199+2106del
XR_927132.1:n.252-5432_252-5429del
XM_017012771.2:c.199+2103_199+2106del	XP_016868260.1:n.199+2103_199+2106del
NM_003930.5:c.199+2103_199+2106del MANE Select	NP_003921.2:n.199+2103_199+2106del
NM_001303468.2:c.-318+2103_-318+2106del	NP_001290397.1:n.-318+2103_-318+2106del