Canonical Allele Identifier: CA2840515368

Gene: GAMT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399758del , CM000681.2:g.1399758del	GRCh38
NC_000019.9:g.1399757del , CM000681.1:g.1399757del	GRCh37
NC_000019.8:g.1350757del	NCBI36
NG_009785.1:g.6796del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.327+35del MANE Select	ENSP00000252288.1:n.327+35del
ENST00000447102.8:c.327+35del	ENSP00000403536.2:n.327+35del
ENST00000591788.3:c.10+35del
ENST00000640762.1:c.258+35del	ENSP00000492031.1:n.258+35del
ENST00000252288.6:c.327+35del	ENSP00000252288.1:n.327+35del
ENST00000447102.7:c.327+35del	ENSP00000403536.2:n.327+35del
ENST00000591788.2:c.12+35del	ENSP00000466341.2:n.12+35del
NM_000156.5:c.327+35del	NP_000147.1:n.327+35del
NM_138924.2:c.327+35del	NP_620279.1:n.327+35del
NM_000156.6:c.327+35del MANE Select	NP_000147.1:n.327+35del
NM_138924.3:c.327+35del	NP_620279.1:n.327+35del