Canonical Allele Identifier: CA2582641948
Gene: GAMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401496_1401506del , CM000681.2:g.1401496_1401506del GRCh38
NC_000019.9:g.1401495_1401505del , CM000681.1:g.1401495_1401505del GRCh37
NC_000019.8:g.1352495_1352505del NCBI36
NG_009785.1:g.5051_5061del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.-27_-17del MANE Select ENSP00000252288.1:n.-27_-17del
ENST00000447102.8:c.-27_-17del ENSP00000403536.2:n.-27_-17del
ENST00000252288.6:c.-27_-17del ENSP00000252288.1:n.-27_-17del
ENST00000447102.7:c.-27_-17del ENSP00000403536.2:n.-27_-17del
NM_000156.5:c.-27_-17del NP_000147.1:n.-27_-17del
NM_138924.2:c.-27_-17del NP_620279.1:n.-27_-17del
NM_000156.6:c.-27_-17del MANE Select NP_000147.1:n.-27_-17del
NM_138924.3:c.-27_-17del NP_620279.1:n.-27_-17del