Canonical Allele Identifier: CA402996417
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1399845-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399845T>C , CM000681.2:g.1399845T>C GRCh38
NC_000019.9:g.1399844T>C , CM000681.1:g.1399844T>C GRCh37
NC_000019.8:g.1350844T>C NCBI36
NG_009785.1:g.6709A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.275A>G MANE Select ENSP00000252288.1:p.Asn92Ser
ENST00000447102.8:c.275A>G ENSP00000403536.2:p.Asn92Ser
ENST00000640762.1:c.206A>G ENSP00000492031.1:p.Asn69Ser
ENST00000252288.6:c.275A>G ENSP00000252288.1:p.Asn92Ser
ENST00000447102.7:c.275A>G ENSP00000403536.2:p.Asn92Ser
NM_000156.5:c.275A>G NP_000147.1:p.Asn92Ser
NM_138924.2:c.275A>G NP_620279.1:p.Asn92Ser
NM_000156.6:c.275A>G MANE Select NP_000147.1:p.Asn92Ser
NM_138924.3:c.275A>G NP_620279.1:p.Asn92Ser