Canonical Allele Identifier: CA2838207655

Gene: ADGRD1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131004489_131004490insA , CM000674.2:g.131004489_131004490insA	GRCh38
NC_000012.11:g.131489034_131489035insA , CM000674.1:g.131489034_131489035insA	GRCh37
NC_000012.10:g.130054987_130054988insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261654.10:c.1255+193_1255+194insA MANE Select	ENSP00000261654.5:n.1255+193_1255+194insA
ENST00000261654.9:c.1255+193_1255+194insA	ENSP00000261654.5:n.1255+193_1255+194insA
ENST00000376682.8:n.568+193_568+194insA
ENST00000535015.5:c.1351+193_1351+194insA	ENSP00000444425.1:n.1351+193_1351+194insA
ENST00000544673.5:n.397+193_397+194insA
ENST00000545900.5:n.400+193_400+194insA
NM_198827.3:c.1255+193_1255+194insA	NP_942122.2:n.1255+193_1255+194insA
XM_005253566.1:c.1075+193_1075+194insA	XP_005253623.1:n.1075+193_1075+194insA
XM_011538203.1:c.1351+193_1351+194insA	XP_011536505.1:n.1351+193_1351+194insA
XM_011538204.1:c.1351+193_1351+194insA	XP_011536506.1:n.1351+193_1351+194insA
XM_011538205.1:c.1171+193_1171+194insA	XP_011536507.1:n.1171+193_1171+194insA
XM_011538206.1:c.1351+193_1351+194insA	XP_011536508.1:n.1351+193_1351+194insA
XM_011538207.1:c.1351+193_1351+194insA	XP_011536509.1:n.1351+193_1351+194insA
XM_011538208.1:c.916+193_916+194insA	XP_011536510.1:n.916+193_916+194insA
XM_011538209.1:c.1351+193_1351+194insA	XP_011536511.1:n.1351+193_1351+194insA
XM_011538210.1:c.1351+193_1351+194insA	XP_011536512.1:n.1351+193_1351+194insA
XM_011538211.1:c.343+193_343+194insA	XP_011536513.1:n.343+193_343+194insA
XM_011538212.1:c.121+193_121+194insA	XP_011536514.1:n.121+193_121+194insA
NM_001330497.1:c.1351+193_1351+194insA	NP_001317426.1:n.1351+193_1351+194insA
NM_198827.4:c.1255+193_1255+194insA	NP_942122.2:n.1255+193_1255+194insA
XM_005253566.2:c.1075+193_1075+194insA	XP_005253623.1:n.1075+193_1075+194insA
XM_011538204.2:c.1351+193_1351+194insA	XP_011536506.1:n.1351+193_1351+194insA
XM_011538205.2:c.1171+193_1171+194insA	XP_011536507.1:n.1171+193_1171+194insA
XM_011538206.2:c.1351+193_1351+194insA	XP_011536508.1:n.1351+193_1351+194insA
XM_011538207.2:c.1351+193_1351+194insA	XP_011536509.1:n.1351+193_1351+194insA
XM_011538208.2:c.916+193_916+194insA	XP_011536510.1:n.916+193_916+194insA
XM_011538209.2:c.1351+193_1351+194insA	XP_011536511.1:n.1351+193_1351+194insA
XM_011538210.2:c.1351+193_1351+194insA	XP_011536512.1:n.1351+193_1351+194insA
XM_011538211.2:c.343+193_343+194insA	XP_011536513.1:n.343+193_343+194insA
XM_011538212.2:c.121+193_121+194insA	XP_011536514.1:n.121+193_121+194insA
NM_198827.5:c.1255+193_1255+194insA MANE Select	NP_942122.2:n.1255+193_1255+194insA
NM_001330497.2:c.1351+193_1351+194insA	NP_001317426.1:n.1351+193_1351+194insA