Canonical Allele Identifier: CA943079854

Gene: GRAMD1B

Linked Data

• dbSNP Id: rs1938446829
• gnomAD v3: 11-123490625-A-AAAT
• gnomAD v4: 11-123490625-A-AAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123490625_123490626insAAT , CM000673.2:g.123490625_123490626insAAT	GRCh38
NC_000011.9:g.123361333_123361334insAAT , CM000673.1:g.123361333_123361334insAAT	GRCh37
NC_000011.8:g.122866543_122866544insAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635736.2:c.452+9732_452+9733insAAT MANE Select	ENSP00000490062.1:n.452+9732_452+9733insAAT
ENST00000635736.1:c.452+9732_452+9733insAAT	ENSP00000490062.1:n.452+9732_452+9733insAAT
ENST00000638157.1:c.-98+9732_-98+9733insAAT	ENSP00000489896.1:n.-98+9732_-98+9733insAAT
ENST00000633087.1:c.92+9732_92+9733insAAT	ENSP00000488613.1:n.92+9732_92+9733insAAT
ENST00000633646.1:c.-98+9732_-98+9733insAAT	ENSP00000488382.1:n.-98+9732_-98+9733insAAT
XM_005271621.3:c.-98+9732_-98+9733insAAT	XP_005271678.1:n.-98+9732_-98+9733insAAT
XM_005271622.3:c.113+9732_113+9733insAAT	XP_005271679.2:n.113+9732_113+9733insAAT
XM_006718892.2:c.152+9732_152+9733insAAT	XP_006718955.1:n.152+9732_152+9733insAAT
XM_011542926.1:c.149+9732_149+9733insAAT	XP_011541228.1:n.149+9732_149+9733insAAT
XM_011542928.1:c.-98+9732_-98+9733insAAT	XP_011541230.1:n.-98+9732_-98+9733insAAT
XM_011542934.1:c.-98+9732_-98+9733insAAT	XP_011541236.1:n.-98+9732_-98+9733insAAT
XM_005271621.4:c.-98+9732_-98+9733insAAT	XP_005271678.1:n.-98+9732_-98+9733insAAT
XM_006718892.3:c.152+9732_152+9733insAAT	XP_006718955.1:n.152+9732_152+9733insAAT
XM_011542926.2:c.149+9732_149+9733insAAT	XP_011541228.1:n.149+9732_149+9733insAAT
XM_017018039.1:c.104+9732_104+9733insAAT	XP_016873528.1:n.104+9732_104+9733insAAT
XM_017018040.1:c.74+70282_74+70283insAAT	XP_016873529.1:n.74+70282_74+70283insAAT
XM_017018041.1:c.104+9732_104+9733insAAT	XP_016873530.1:n.104+9732_104+9733insAAT
XM_017018042.1:c.104+9732_104+9733insAAT	XP_016873531.1:n.104+9732_104+9733insAAT
XM_017018045.1:c.-98+9732_-98+9733insAAT	XP_016873534.1:n.-98+9732_-98+9733insAAT
XM_024448622.1:c.27-86742_27-86741insAAT	XP_024304390.1:n.27-86742_27-86741insAAT
NM_001367418.1:c.104+9732_104+9733insAAT	NP_001354347.1:n.104+9732_104+9733insAAT
NM_001367419.1:c.104+9732_104+9733insAAT	NP_001354348.1:n.104+9732_104+9733insAAT
NM_001367420.1:c.104+9732_104+9733insAAT	NP_001354349.1:n.104+9732_104+9733insAAT
NM_001367421.1:c.320+9732_320+9733insAAT	NP_001354350.1:n.320+9732_320+9733insAAT
NM_001367421.2:c.320+9732_320+9733insAAT	NP_001354350.1:n.320+9732_320+9733insAAT
NM_001367418.2:c.104+9732_104+9733insAAT	NP_001354347.1:n.104+9732_104+9733insAAT
NM_001367419.2:c.104+9732_104+9733insAAT	NP_001354348.1:n.104+9732_104+9733insAAT
NM_001367420.2:c.104+9732_104+9733insAAT	NP_001354349.1:n.104+9732_104+9733insAAT
NM_001387024.1:c.452+9732_452+9733insAAT	NP_001373953.1:n.452+9732_452+9733insAAT
NM_001387025.1:c.452+9732_452+9733insAAT MANE Select	NP_001373954.1:n.452+9732_452+9733insAAT
NM_001387026.1:c.449+9732_449+9733insAAT	NP_001373955.1:n.449+9732_449+9733insAAT
NM_001387030.1:c.-98+9732_-98+9733insAAT	NP_001373959.1:n.-98+9732_-98+9733insAAT
NM_001387034.1:c.-98+9732_-98+9733insAAT	NP_001373963.1:n.-98+9732_-98+9733insAAT