Canonical Allele Identifier: CA2317700534
Gene: GAMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401531C= , CM000681.2:g.1401531C= GRCh38
NC_000019.9:g.1401530C= , CM000681.1:g.1401530C= GRCh37
NC_000019.8:g.1352530C= NCBI36
NG_009785.1:g.5023G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.-55G= MANE Select ENSP00000252288.1:n.-55G=
ENST00000447102.8:c.-55G= ENSP00000403536.2:n.-55G=
ENST00000252288.6:c.-55G= ENSP00000252288.1:n.-55G=
ENST00000447102.7:c.-55G= ENSP00000403536.2:n.-55G=
NM_000156.5:c.-55G= NP_000147.1:n.-55G=
NM_138924.2:c.-55G= NP_620279.1:n.-55G=
NM_000156.6:c.-55G= MANE Select NP_000147.1:n.-55G=
NM_138924.3:c.-55G= NP_620279.1:n.-55G=
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