Canonical Allele Identifier: CA2813256108
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401191_1401193del , CM000681.2:g.1401191_1401193del GRCh38
NC_000019.9:g.1401190_1401192del , CM000681.1:g.1401190_1401192del GRCh37
NC_000019.8:g.1352190_1352192del NCBI36
NG_009785.1:g.5362_5364del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.181+104_181+106del MANE Select ENSP00000252288.1:n.181+104_181+106del
ENST00000447102.8:c.181+104_181+106del ENSP00000403536.2:n.181+104_181+106del
ENST00000640762.1:c.112+173_112+175del ENSP00000492031.1:n.112+173_112+175del
ENST00000252288.6:c.181+104_181+106del ENSP00000252288.1:n.181+104_181+106del
ENST00000447102.7:c.181+104_181+106del ENSP00000403536.2:n.181+104_181+106del
NM_000156.5:c.181+104_181+106del NP_000147.1:n.181+104_181+106del
NM_138924.2:c.181+104_181+106del NP_620279.1:n.181+104_181+106del
NM_000156.6:c.181+104_181+106del MANE Select NP_000147.1:n.181+104_181+106del
NM_138924.3:c.181+104_181+106del NP_620279.1:n.181+104_181+106del