Canonical Allele Identifier: CA389265086
Gene: TGM1 HGNC NCBI

Linked Data

gnomAD v4: 14-24259200-T-G
MyVariant Identifiers: chr14:g.24728406T>G (hg19) chr14:g.24259200T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259200T>G , CM000676.2:g.24259200T>G GRCh38
NC_000014.8:g.24728406T>G , CM000676.1:g.24728406T>G GRCh37
NC_000014.7:g.23798246T>G NCBI36
NG_007150.1:g.8967A>C
NG_007150.2:g.8967A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1034A>C MANE Select ENSP00000206765.6:p.Asp345Ala
ENST00000206765.10:c.1034A>C ENSP00000206765.6:p.Asp345Ala
ENST00000544573.5:c.-28-812A>C ENSP00000439446.1:n.-28-812A>C
ENST00000559136.1:c.107A>C ENSP00000453337.1:p.Asp36Ala
NM_000359.2:c.1034A>C NP_000350.1:p.Asp345Ala
NM_000359.3:c.1034A>C MANE Select NP_000350.1:p.Asp345Ala
Search 100 bp 5'
Search 100 bp 3'