Canonical Allele Identifier: CA1788923379
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038804_63038808delinsTGCGG , CM000670.2:g.63038804_63038808delinsTGCGG GRCh38
NC_000008.10:g.63951363_63951367delinsTGCGG , CM000670.1:g.63951363_63951367delinsTGCGG GRCh37
NC_000008.9:g.64113917_64113921delinsTGCGG NCBI36
NG_028126.1:g.5244_5248delinsCCGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000677327.1:n.600_604delinsCCGCA
ENST00000677482.1:c.-40_-36delinsCCGCA ENSP00000504590.1:n.-40_-36delinsCCGCA
ENST00000679326.1:c.-40_-36delinsCCGCA ENSP00000504262.1:n.-40_-36delinsCCGCA
ENST00000260118.6:c.-40_-36delinsCCGCA ENSP00000260118.6:n.-40_-36delinsCCGCA
NM_003878.2:c.-40_-36delinsCCGCA NP_003869.1:n.-40_-36delinsCCGCA
XM_011517623.1:c.-40_-36delinsCCGCA XP_011515925.1:n.-40_-36delinsCCGCA