Canonical Allele Identifier: CA402994988
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399137T>G (hg19) chr19:g.1399138T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399138T>G , CM000681.2:g.1399138T>G GRCh38
NC_000019.9:g.1399137T>G , CM000681.1:g.1399137T>G GRCh37
NC_000019.8:g.1350137T>G NCBI36
NG_009785.1:g.7416A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.449A>C MANE Select ENSP00000252288.1:p.Asn150Thr
ENST00000447102.8:c.449A>C ENSP00000403536.2:p.Asn150Thr
ENST00000591788.3:c.132A>C
ENST00000640164.1:n.282A>C
ENST00000640762.1:c.380A>C ENSP00000492031.1:p.Asn127Thr
ENST00000252288.6:c.449A>C ENSP00000252288.1:p.Asn150Thr
ENST00000447102.7:c.449A>C ENSP00000403536.2:p.Asn150Thr
ENST00000591788.2:c.134A>C ENSP00000466341.2:p.Asn45Thr
NM_000156.5:c.449A>C NP_000147.1:p.Asn150Thr
NM_138924.2:c.449A>C NP_620279.1:p.Asn150Thr
NM_000156.6:c.449A>C MANE Select NP_000147.1:p.Asn150Thr
NM_138924.3:c.449A>C NP_620279.1:p.Asn150Thr
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