Canonical Allele Identifier: CA2873880
Community Standard Title: NM_145290.4(ADGRA3):c.1659G>C (p.Thr553=)
Gene: ADGRA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.22421036C>G , CM000666.2:g.22421036C>G GRCh38
NC_000004.11:g.22422659C>G , CM000666.1:g.22422659C>G GRCh37
NC_000004.10:g.22031757C>G NCBI36
NG_032963.1:g.100019G>C

Transcript Alleles

HGVS Amino-acid Change
NM_145290.4:c.1659G>C MANE Select NP_660333.2:p.Thr553=
ENST00000334304.10:c.1659G>C MANE Select ENSP00000334952.5:p.Thr553=
NM_145290.3:c.1659G>C NP_660333.2:p.Thr553=
ENST00000282943.9:n.1284G>C
ENST00000334304.9:c.1659G>C ENSP00000334952.5:p.Thr553=
ENST00000502482.1:c.1659G>C ENSP00000421006.1:p.Thr553=
ENST00000508133.5:c.981G>C ENSP00000422606.1:p.Thr327=
XM_005248137.3:c.1659G>C XP_005248194.1:p.Thr553=
XM_005248137.5:c.1659G>C XP_005248194.1:p.Thr553=
XM_011513810.1:c.1068G>C XP_011512112.1:p.Thr356=
XM_011513811.1:c.981G>C XP_011512113.1:p.Thr327=
XM_011513811.2:c.981G>C XP_011512113.1:p.Thr327=
XR_001741153.1:n.1933G>C
XR_925316.1:n.1933G>C