Canonical Allele Identifier: CA389277144
Gene: TGM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.24730934A>G (hg19) chr14:g.24261728A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261728A>G , CM000676.2:g.24261728A>G GRCh38
NC_000014.8:g.24730934A>G , CM000676.1:g.24730934A>G GRCh37
NC_000014.7:g.23800774A>G NCBI36
NG_007150.1:g.6439T>C
NG_007150.2:g.6439T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.475T>C MANE Select ENSP00000206765.6:p.Ser159Pro
ENST00000206765.10:c.475T>C ENSP00000206765.6:p.Ser159Pro
ENST00000544573.5:c.-29+399T>C ENSP00000439446.1:n.-29+399T>C
NM_000359.2:c.475T>C NP_000350.1:p.Ser159Pro
NM_000359.3:c.475T>C MANE Select NP_000350.1:p.Ser159Pro
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