Canonical Allele Identifier: CA2695223160
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399836_1399838dup , CM000681.2:g.1399836_1399838dup GRCh38
NC_000019.9:g.1399835_1399837dup , CM000681.1:g.1399835_1399837dup GRCh37
NC_000019.8:g.1350835_1350837dup NCBI36
NG_009785.1:g.6717_6719dup

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.283_285dup MANE Select ENSP00000252288.1:p.Val95_Phe96insVal
ENST00000447102.8:c.283_285dup ENSP00000403536.2:p.Val95_Phe96insVal
ENST00000640762.1:c.214_216dup ENSP00000492031.1:p.Val72_Phe73insVal
ENST00000252288.6:c.283_285dup ENSP00000252288.1:p.Val95_Phe96insVal
ENST00000447102.7:c.283_285dup ENSP00000403536.2:p.Val95_Phe96insVal
NM_000156.5:c.283_285dup NP_000147.1:p.Val95_Phe96insVal
NM_138924.2:c.283_285dup NP_620279.1:p.Val95_Phe96insVal
NM_000156.6:c.283_285dup MANE Select NP_000147.1:p.Val95_Phe96insVal
NM_138924.3:c.283_285dup NP_620279.1:p.Val95_Phe96insVal