Canonical Allele Identifier: CA402996122

Gene: GAMT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399804G>A , CM000681.2:g.1399804G>A	GRCh38
NC_000019.9:g.1399803G>A , CM000681.1:g.1399803G>A	GRCh37
NC_000019.8:g.1350803G>A	NCBI36
NG_009785.1:g.6750C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000156.6:c.316C>T MANE Select	NP_000147.1:p.Gln106Ter
ENST00000252288.8:c.316C>T MANE Select	ENSP00000252288.1:p.Gln106Ter
NM_000156.5:c.316C>T	NP_000147.1:p.Gln106Ter
NM_138924.2:c.316C>T	NP_620279.1:p.Gln106Ter
NM_138924.3:c.316C>T	NP_620279.1:p.Gln106Ter
ENST00000252288.6:c.316C>T	ENSP00000252288.1:p.Gln106Ter
ENST00000447102.7:c.316C>T	ENSP00000403536.2:p.Gln106Ter
ENST00000447102.8:c.316C>T	ENSP00000403536.2:p.Gln106Ter
ENST00000591788.2:c.1C>T	ENSP00000466341.2:p.Gln1Ter
ENST00000640762.1:c.247C>T	ENSP00000492031.1:p.Gln83Ter