Canonical Allele Identifier: CA402995271
Gene: GAMT HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1399167G>C (hg19) chr19:g.1399168G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399168G>C , CM000681.2:g.1399168G>C GRCh38
NC_000019.9:g.1399167G>C , CM000681.1:g.1399167G>C GRCh37
NC_000019.8:g.1350167G>C NCBI36
NG_009785.1:g.7386C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.419C>G MANE Select ENSP00000252288.1:p.Ser140Trp
ENST00000447102.8:c.419C>G ENSP00000403536.2:p.Ser140Trp
ENST00000591788.3:c.102C>G
ENST00000640164.1:n.252C>G
ENST00000640762.1:c.350C>G ENSP00000492031.1:p.Ser117Trp
ENST00000252288.6:c.419C>G ENSP00000252288.1:p.Ser140Trp
ENST00000447102.7:c.419C>G ENSP00000403536.2:p.Ser140Trp
ENST00000591788.2:c.104C>G ENSP00000466341.2:p.Ser35Trp
NM_000156.5:c.419C>G NP_000147.1:p.Ser140Trp
NM_138924.2:c.419C>G NP_620279.1:p.Ser140Trp
NM_000156.6:c.419C>G MANE Select NP_000147.1:p.Ser140Trp
NM_138924.3:c.419C>G NP_620279.1:p.Ser140Trp
Search 100 bp 5'
Search 100 bp 3'