Canonical Allele Identifier: CA2582641927

Gene: GAMT

Linked Data

• gnomAD v4: 19-1401422-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1401426del , CM000681.2:g.1401426del	GRCh38
NC_000019.9:g.1401425del , CM000681.1:g.1401425del	GRCh37
NC_000019.8:g.1352425del	NCBI36
NG_009785.1:g.5131del

Transcript Alleles

HGVS	Amino-acid change
ENST00000252288.8:c.54del MANE Select	ENSP00000252288.1:p.Ala19ArgfsTer23
ENST00000447102.8:c.54del	ENSP00000403536.2:p.Ala19ArgfsTer23
ENST00000640762.1:c.54del	ENSP00000492031.1:p.Ala19ArgfsTer?
ENST00000252288.6:c.54del	ENSP00000252288.1:p.Ala19ArgfsTer23
ENST00000447102.7:c.54del	ENSP00000403536.2:p.Ala19ArgfsTer23
NM_000156.5:c.54del	NP_000147.1:p.Ala19ArgfsTer23
NM_138924.2:c.54del	NP_620279.1:p.Ala19ArgfsTer23
NM_000156.6:c.54del MANE Select	NP_000147.1:p.Ala19ArgfsTer23
NM_138924.3:c.54del	NP_620279.1:p.Ala19ArgfsTer23