Canonical Allele Identifier: CA1788923607
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63039092_63039097delinsCCCTTT , CM000670.2:g.63039092_63039097delinsCCCTTT GRCh38
NC_000008.10:g.63951651_63951656delinsCCCTTT , CM000670.1:g.63951651_63951656delinsCCCTTT GRCh37
NC_000008.9:g.64114205_64114210delinsCCCTTT NCBI36
NG_028126.1:g.4955_4960delinsAAAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.311_316delinsAAAGGG
ENST00000679326.1:c.-329_-324delinsAAAGGG ENSP00000504262.1:n.-329_-324delinsAAAGGG
ENST00000260118.6:c.-329_-324delinsAAAGGG ENSP00000260118.6:n.-329_-324delinsAAAGGG
XM_011517623.1:c.-329_-324delinsAAAGGG XP_011515925.1:n.-329_-324delinsAAAGGG