Canonical Allele Identifier: CA1777263968

Gene: ADGRA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37823972T= , CM000670.2:g.37823972T=	GRCh38
NC_000008.10:g.37681490T= , CM000670.1:g.37681490T=	GRCh37
NC_000008.9:g.37800648T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000412232.3:c.339-4916T= MANE Select	ENSP00000406367.2:n.339-4916T=
ENST00000315215.11:c.339-4916T=	ENSP00000323508.7:n.339-4916T=
ENST00000412232.2:c.339-4916T=	ENSP00000406367.2:n.339-4916T=
ENST00000428068.5:c.213-4916T=	ENSP00000400860.1:n.213-4916T=
NM_032777.9:c.339-4916T=	NP_116166.9:n.339-4916T=
XM_005273471.3:c.339-4916T=	XP_005273528.1:n.339-4916T=
XM_011544481.1:c.339-4916T=	XP_011542783.1:n.339-4916T=
XM_011544482.1:c.267-4916T=	XP_011542784.1:n.267-4916T=
XM_011544483.1:c.339-4916T=	XP_011542785.1:n.339-4916T=
XM_011544481.2:c.339-4916T=	XP_011542783.1:n.339-4916T=
XM_011544482.2:c.267-4916T=	XP_011542784.1:n.267-4916T=
XM_011544483.2:c.339-4916T=	XP_011542785.1:n.339-4916T=
NM_032777.10:c.339-4916T= MANE Select	NP_116166.9:n.339-4916T=