Canonical Allele Identifier: CA2323580653

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12806788_12806789delinsGG , CM000681.2:g.12806788_12806789delinsGG GRCh38
NC_000019.9:g.12917602_12917603delinsGG , CM000681.1:g.12917602_12917603delinsGG GRCh37
NC_000019.8:g.12778602_12778603delinsGG NCBI36
NG_012662.1:g.5175_5176delinsGG , LRG_278:g.5175_5176delinsGG
NG_029901.1:g.92_93delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000221486.6:c.115_116delinsGG (RNASEH2A) MANE Select ENSP00000221486.4:p.Gly39=
ENST00000590121.2:c.112_113delinsGG (RNASEH2A) ENSP00000495087.1:p.Gly38=
ENST00000590279.2:n.197_198delinsGG (RNASEH2A)
ENST00000593017.2:n.105_106delinsGG (RNASEH2A)
ENST00000639767.2:c.*7-220_*7-219delinsGG (THSD8) ENSP00000491410.2:n.*7-220_*7-219delinsGG
ENST00000643364.1:n.799_800delinsGG (THSD8)
ENST00000646769.1:c.115_116delinsGG (RNASEH2A) ENSP00000495175.1:p.Gly39=
ENST00000221486.4:c.115_116delinsGG (RNASEH2A) ENSP00000221486.3:p.Gly39=
ENST00000589765.1:n.41+18389_41+18390delinsCC (HOOK2)
ENST00000590121.1:n.112_113delinsGG (RNASEH2A)
ENST00000590279.1:n.105_106delinsGG (RNASEH2A)
ENST00000593017.1:n.197_198delinsGG (RNASEH2A)
NM_006397.2:c.115_116delinsGG , LRG_278t1:c.115_116delinsGG (RNASEH2A) NP_006388.2:p.Gly39=
XM_006722619.2:c.-5-220_-5-219delinsGG (RNASEH2A) XP_006722682.1:n.-5-220_-5-219delinsGG
NM_006397.3:c.115_116delinsGG (RNASEH2A) MANE Select NP_006388.2:p.Gly39=