Canonical Allele Identifier: CA1788923509
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038958_63038969delinsAGCCGGCGCTGC , CM000670.2:g.63038958_63038969delinsAGCCGGCGCTGC GRCh38
NC_000008.10:g.63951517_63951528delinsAGCCGGCGCTGC , CM000670.1:g.63951517_63951528delinsAGCCGGCGCTGC GRCh37
NC_000008.9:g.64114071_64114082delinsAGCCGGCGCTGC NCBI36
NG_028126.1:g.5083_5094delinsGCAGCGCCGGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.439_450delinsGCAGCGCCGGCT
ENST00000679326.1:c.-201_-190delinsGCAGCGCCGGCT ENSP00000504262.1:n.-201_-190delinsGCAGCGCCGGCT
ENST00000260118.6:c.-201_-190delinsGCAGCGCCGGCT ENSP00000260118.6:n.-201_-190delinsGCAGCGCCGGCT
NM_003878.2:c.-201_-190delinsGCAGCGCCGGCT NP_003869.1:n.-201_-190delinsGCAGCGCCGGCT
XM_011517623.1:c.-201_-190delinsGCAGCGCCGGCT XP_011515925.1:n.-201_-190delinsGCAGCGCCGGCT