Canonical Allele Identifier: CA1777263958
Gene: ADGRA2 HGNC NCBI

Linked Data

dbSNP Id: rs1805195955

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37823958del , CM000670.2:g.37823958del GRCh38
NC_000008.10:g.37681476del , CM000670.1:g.37681476del GRCh37
NC_000008.9:g.37800634del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000412232.3:c.339-4930del MANE Select ENSP00000406367.2:n.339-4930del
ENST00000315215.11:c.339-4930del ENSP00000323508.7:n.339-4930del
ENST00000412232.2:c.339-4930del ENSP00000406367.2:n.339-4930del
ENST00000428068.5:c.213-4930del ENSP00000400860.1:n.213-4930del
NM_032777.9:c.339-4930del NP_116166.9:n.339-4930del
XM_005273471.3:c.339-4930del XP_005273528.1:n.339-4930del
XM_011544481.1:c.339-4930del XP_011542783.1:n.339-4930del
XM_011544482.1:c.267-4930del XP_011542784.1:n.267-4930del
XM_011544483.1:c.339-4930del XP_011542785.1:n.339-4930del
XM_011544481.2:c.339-4930del XP_011542783.1:n.339-4930del
XM_011544482.2:c.267-4930del XP_011542784.1:n.267-4930del
XM_011544483.2:c.339-4930del XP_011542785.1:n.339-4930del
NM_032777.10:c.339-4930del MANE Select NP_116166.9:n.339-4930del