Canonical Allele Identifier: CA2813256109
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401199dup , CM000681.2:g.1401199dup GRCh38
NC_000019.9:g.1401198dup , CM000681.1:g.1401198dup GRCh37
NC_000019.8:g.1352198dup NCBI36
NG_009785.1:g.5358dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.181+100dup MANE Select ENSP00000252288.1:n.181+100dup
ENST00000447102.8:c.181+100dup ENSP00000403536.2:n.181+100dup
ENST00000640762.1:c.112+169dup ENSP00000492031.1:n.112+169dup
ENST00000252288.6:c.181+100dup ENSP00000252288.1:n.181+100dup
ENST00000447102.7:c.181+100dup ENSP00000403536.2:n.181+100dup
NM_000156.5:c.181+100dup NP_000147.1:n.181+100dup
NM_138924.2:c.181+100dup NP_620279.1:n.181+100dup
NM_000156.6:c.181+100dup MANE Select NP_000147.1:n.181+100dup
NM_138924.3:c.181+100dup NP_620279.1:n.181+100dup