Canonical Allele Identifier: CA2072219773

Gene: ADGRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131137217A>C , CM000674.2:g.131137217A>C	GRCh38
NC_000012.11:g.131621762A>C , CM000674.1:g.131621762A>C	GRCh37
NC_000012.10:g.130187715A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261654.10:c.2436+203A>C MANE Select	ENSP00000261654.5:n.2436+203A>C
ENST00000261654.9:c.2436+203A>C	ENSP00000261654.5:n.2436+203A>C
ENST00000335486.10:c.282+203A>C	ENSP00000334127.7:n.282+203A>C
ENST00000376682.8:n.1749+203A>C
ENST00000446583.6:c.786+203A>C	ENSP00000482235.1:n.786+203A>C
ENST00000535015.5:c.2532+203A>C	ENSP00000444425.1:n.2532+203A>C
ENST00000540207.1:n.303+203A>C
ENST00000543617.2:c.993+203A>C	ENSP00000438021.1:n.993+203A>C
NM_198827.3:c.2436+203A>C	NP_942122.2:n.2436+203A>C
XM_005253566.1:c.2256+203A>C	XP_005253623.1:n.2256+203A>C
XM_011538203.1:c.2532+203A>C	XP_011536505.1:n.2532+203A>C
XM_011538204.1:c.2532+203A>C	XP_011536506.1:n.2532+203A>C
XM_011538205.1:c.2352+203A>C	XP_011536507.1:n.2352+203A>C
XM_011538206.1:c.2316+203A>C	XP_011536508.1:n.2316+203A>C
XM_011538208.1:c.2097+203A>C	XP_011536510.1:n.2097+203A>C
XM_011538209.1:c.2028+203A>C	XP_011536511.1:n.2028+203A>C
XM_011538211.1:c.1524+203A>C	XP_011536513.1:n.1524+203A>C
XM_011538212.1:c.1302+203A>C	XP_011536514.1:n.1302+203A>C
NM_001330497.1:c.2532+203A>C	NP_001317426.1:n.2532+203A>C
NM_198827.4:c.2436+203A>C	NP_942122.2:n.2436+203A>C
XM_005253566.2:c.2256+203A>C	XP_005253623.1:n.2256+203A>C
XM_011538204.2:c.2532+203A>C	XP_011536506.1:n.2532+203A>C
XM_011538205.2:c.2352+203A>C	XP_011536507.1:n.2352+203A>C
XM_011538206.2:c.2316+203A>C	XP_011536508.1:n.2316+203A>C
XM_011538208.2:c.2097+203A>C	XP_011536510.1:n.2097+203A>C
XM_011538209.2:c.2028+203A>C	XP_011536511.1:n.2028+203A>C
XM_011538211.2:c.1524+203A>C	XP_011536513.1:n.1524+203A>C
XM_011538212.2:c.1302+203A>C	XP_011536514.1:n.1302+203A>C
NM_198827.5:c.2436+203A>C MANE Select	NP_942122.2:n.2436+203A>C
NM_001330497.2:c.2532+203A>C	NP_001317426.1:n.2532+203A>C