Canonical Allele Identifier: CA2317700522

Gene: GAMT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1401518C= , CM000681.2:g.1401518C=	GRCh38
NC_000019.9:g.1401517C= , CM000681.1:g.1401517C=	GRCh37
NC_000019.8:g.1352517C=	NCBI36
NG_009785.1:g.5036G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.-42G= MANE Select	ENSP00000252288.1:n.-42G=
ENST00000447102.8:c.-42G=	ENSP00000403536.2:n.-42G=
ENST00000252288.6:c.-42G=	ENSP00000252288.1:n.-42G=
ENST00000447102.7:c.-42G=	ENSP00000403536.2:n.-42G=
NM_000156.5:c.-42G=	NP_000147.1:n.-42G=
NM_138924.2:c.-42G=	NP_620279.1:n.-42G=
NM_000156.6:c.-42G= MANE Select	NP_000147.1:n.-42G=
NM_138924.3:c.-42G=	NP_620279.1:n.-42G=