Canonical Allele Identifier: CA1114587548
Gene: GGH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038857del , CM000670.2:g.63038857del GRCh38
NC_000008.10:g.63951416del , CM000670.1:g.63951416del GRCh37
NC_000008.9:g.64113970del NCBI36
NG_028126.1:g.5195del

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.551del
ENST00000677482.1:c.-89del ENSP00000504590.1:n.-89del
ENST00000679326.1:c.-89del ENSP00000504262.1:n.-89del
ENST00000260118.6:c.-89del ENSP00000260118.6:n.-89del
NM_003878.2:c.-89del NP_003869.1:n.-89del
XM_011517623.1:c.-89del XP_011515925.1:n.-89del