Canonical Allele Identifier: CA2780586680
Gene: GGH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63038993_63038994insACA , CM000670.2:g.63038993_63038994insACA GRCh38
NC_000008.10:g.63951552_63951553insACA , CM000670.1:g.63951552_63951553insACA GRCh37
NC_000008.9:g.64114106_64114107insACA NCBI36
NG_028126.1:g.5058_5059insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000677327.1:n.414_415insTGT
ENST00000679326.1:c.-226_-225insTGT ENSP00000504262.1:n.-226_-225insTGT
ENST00000260118.6:c.-226_-225insTGT ENSP00000260118.6:n.-226_-225insTGT
NM_003878.2:c.-226_-225insTGT NP_003869.1:n.-226_-225insTGT
XM_011517623.1:c.-226_-225insTGT XP_011515925.1:n.-226_-225insTGT