Canonical Allele Identifier: CA389269341
Gene: TGM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.24729145C>A (hg19) chr14:g.24259939C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259939C>A , CM000676.2:g.24259939C>A GRCh38
NC_000014.8:g.24729145C>A , CM000676.1:g.24729145C>A GRCh37
NC_000014.7:g.23798985C>A NCBI36
NG_007150.1:g.8228G>T
NG_007150.2:g.8228G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.876+1G>T MANE Select ENSP00000206765.6:n.876+1G>T
ENST00000206765.10:c.876+1G>T ENSP00000206765.6:n.876+1G>T
ENST00000544573.5:c.-28-1551G>T ENSP00000439446.1:n.-28-1551G>T
ENST00000559136.1:c.-52+1G>T ENSP00000453337.1:n.-52+1G>T
NM_000359.2:c.876+1G>T NP_000350.1:n.876+1G>T
NM_000359.3:c.876+1G>T MANE Select NP_000350.1:n.876+1G>T
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