Canonical Allele Identifier: CA1668776508
Gene: ADGRG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.142382916_142382919delinsCATT , CM000668.2:g.142382916_142382919delinsCATT GRCh38
NC_000006.11:g.142704053_142704056delinsCATT , CM000668.1:g.142704053_142704056delinsCATT GRCh37
NC_000006.10:g.142745746_142745749delinsCATT NCBI36
NG_011839.1:g.85998_86001delinsCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000296932.13:c.1138+897_1138+900delinsCATT ENSP00000296932.8:n.1138+897_1138+900delinsCATT
ENST00000367609.8:c.1139-844_1139-841delinsCATT MANE Select ENSP00000356581.3:n.1139-844_1139-841delinsCATT
ENST00000230173.10:c.1139-844_1139-841delinsCATT ENSP00000230173.6:n.1139-844_1139-841delinsCATT
ENST00000296932.12:c.1138+897_1138+900delinsCATT ENSP00000296932.8:n.1138+897_1138+900delinsCATT
ENST00000367608.6:c.1138+897_1138+900delinsCATT ENSP00000356580.2:n.1138+897_1138+900delinsCATT
ENST00000367609.7:c.1139-844_1139-841delinsCATT ENSP00000356581.3:n.1139-844_1139-841delinsCATT
NM_001032394.2:c.1138+897_1138+900delinsCATT NP_001027566.1:n.1138+897_1138+900delinsCATT
NM_001032395.2:c.1138+897_1138+900delinsCATT NP_001027567.1:n.1138+897_1138+900delinsCATT
NM_020455.5:c.1139-844_1139-841delinsCATT NP_065188.4:n.1139-844_1139-841delinsCATT
NM_198569.2:c.1139-844_1139-841delinsCATT NP_940971.1:n.1139-844_1139-841delinsCATT
XM_005267061.2:c.1142-844_1142-841delinsCATT XP_005267118.1:n.1142-844_1142-841delinsCATT
XM_006715516.2:c.1142-844_1142-841delinsCATT XP_006715579.1:n.1142-844_1142-841delinsCATT
XM_006715517.2:c.1136-844_1136-841delinsCATT XP_006715580.1:n.1136-844_1136-841delinsCATT
XM_006715518.2:c.1141+897_1141+900delinsCATT XP_006715581.1:n.1141+897_1141+900delinsCATT
XM_011535964.1:c.1139-844_1139-841delinsCATT XP_011534266.1:n.1139-844_1139-841delinsCATT
XM_005267061.3:c.1142-844_1142-841delinsCATT XP_005267118.1:n.1142-844_1142-841delinsCATT
XM_017011085.1:c.1142-844_1142-841delinsCATT XP_016866574.1:n.1142-844_1142-841delinsCATT
NM_198569.3:c.1139-844_1139-841delinsCATT MANE Select NP_940971.2:n.1139-844_1139-841delinsCATT
NM_001032394.3:c.1138+897_1138+900delinsCATT NP_001027566.2:n.1138+897_1138+900delinsCATT
NM_001032395.3:c.1138+897_1138+900delinsCATT NP_001027567.2:n.1138+897_1138+900delinsCATT
NM_020455.6:c.1139-844_1139-841delinsCATT NP_065188.5:n.1139-844_1139-841delinsCATT