Canonical Allele Identifier: CA2582641478

Gene: GAMT

Linked Data

• gnomAD v4: 19-1399783-A-ACAC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399783_1399784insCAC , CM000681.2:g.1399783_1399784insCAC	GRCh38
NC_000019.9:g.1399782_1399783insCAC , CM000681.1:g.1399782_1399783insCAC	GRCh37
NC_000019.8:g.1350782_1350783insCAC	NCBI36
NG_009785.1:g.6770_6771insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.327+9_327+10insGTG MANE Select	ENSP00000252288.1:n.327+9_327+10insGTG
ENST00000447102.8:c.327+9_327+10insGTG	ENSP00000403536.2:n.327+9_327+10insGTG
ENST00000591788.3:c.10+9_10+10insGTG
ENST00000640762.1:c.258+9_258+10insGTG	ENSP00000492031.1:n.258+9_258+10insGTG
ENST00000252288.6:c.327+9_327+10insGTG	ENSP00000252288.1:n.327+9_327+10insGTG
ENST00000447102.7:c.327+9_327+10insGTG	ENSP00000403536.2:n.327+9_327+10insGTG
ENST00000591788.2:c.12+9_12+10insGTG	ENSP00000466341.2:n.12+9_12+10insGTG
NM_000156.5:c.327+9_327+10insGTG	NP_000147.1:n.327+9_327+10insGTG
NM_138924.2:c.327+9_327+10insGTG	NP_620279.1:n.327+9_327+10insGTG
NM_000156.6:c.327+9_327+10insGTG MANE Select	NP_000147.1:n.327+9_327+10insGTG
NM_138924.3:c.327+9_327+10insGTG	NP_620279.1:n.327+9_327+10insGTG