Canonical Allele Identifier: CA2509220625
Gene: GREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240558277_240558278insAAAT , CM000663.2:g.240558277_240558278insAAAT GRCh38
NC_000001.10:g.240721577_240721578insAAAT , CM000663.1:g.240721577_240721578insAAAT GRCh37
NC_000001.9:g.238788200_238788201insAAAT NCBI36
NG_053136.1:g.59095_59096insATTT

Transcript Alleles

HGVS Amino-acid change
ENST00000318160.5:c.-2+53606_-2+53607insATTT MANE Select ENSP00000318650.4:n.-2+53606_-2+53607insATTT
ENST00000318160.4:c.-2+53606_-2+53607insATTT ENSP00000318650.4:n.-2+53606_-2+53607insATTT
NM_022469.3:c.-2+53606_-2+53607insATTT NP_071914.3:n.-2+53606_-2+53607insATTT
XM_011544249.1:c.-122+53606_-122+53607insATTT XP_011542551.1:n.-122+53606_-122+53607insATTT
XR_949319.1:n.219+2065_219+2066insAAAT
XM_011544249.2:c.-122+53606_-122+53607insATTT XP_011542551.1:n.-122+53606_-122+53607insATTT
NM_022469.4:c.-2+53606_-2+53607insATTT MANE Select NP_071914.3:n.-2+53606_-2+53607insATTT