Canonical Allele Identifier: CA402996307
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1399831-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399831G>T , CM000681.2:g.1399831G>T GRCh38
NC_000019.9:g.1399830G>T , CM000681.1:g.1399830G>T GRCh37
NC_000019.8:g.1350830G>T NCBI36
NG_009785.1:g.6723C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.289C>A MANE Select ENSP00000252288.1:p.Gln97Lys
ENST00000447102.8:c.289C>A ENSP00000403536.2:p.Gln97Lys
ENST00000640762.1:c.220C>A ENSP00000492031.1:p.Gln74Lys
ENST00000252288.6:c.289C>A ENSP00000252288.1:p.Gln97Lys
ENST00000447102.7:c.289C>A ENSP00000403536.2:p.Gln97Lys
NM_000156.5:c.289C>A NP_000147.1:p.Gln97Lys
NM_138924.2:c.289C>A NP_620279.1:p.Gln97Lys
NM_000156.6:c.289C>A MANE Select NP_000147.1:p.Gln97Lys
NM_138924.3:c.289C>A NP_620279.1:p.Gln97Lys