Canonical Allele Identifier: CA402995416
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399190G>C (hg19) chr19:g.1399191G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399191G>C , CM000681.2:g.1399191G>C GRCh38
NC_000019.9:g.1399190G>C , CM000681.1:g.1399190G>C GRCh37
NC_000019.8:g.1350190G>C NCBI36
NG_009785.1:g.7363C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.396C>G MANE Select ENSP00000252288.1:p.Ile132Met
ENST00000447102.8:c.396C>G ENSP00000403536.2:p.Ile132Met
ENST00000591788.3:c.79C>G
ENST00000640164.1:n.229C>G
ENST00000640762.1:c.327C>G ENSP00000492031.1:p.Ile109Met
ENST00000252288.6:c.396C>G ENSP00000252288.1:p.Ile132Met
ENST00000447102.7:c.396C>G ENSP00000403536.2:p.Ile132Met
ENST00000591788.2:c.81C>G ENSP00000466341.2:p.Ile27Met
NM_000156.5:c.396C>G NP_000147.1:p.Ile132Met
NM_138924.2:c.396C>G NP_620279.1:p.Ile132Met
NM_000156.6:c.396C>G MANE Select NP_000147.1:p.Ile132Met
NM_138924.3:c.396C>G NP_620279.1:p.Ile132Met
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