Canonical Allele Identifier: CA2123832081
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs2040746437
gnomAD v3: 14-24255891-AC-A
gnomAD v4: 14-24255891-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24255892del , CM000676.2:g.24255892del GRCh38
NC_000014.8:g.24725098del , CM000676.1:g.24725098del GRCh37
NC_000014.7:g.23794938del NCBI36
NG_007150.1:g.12275del
NG_007150.2:g.12275del

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1491+97del MANE Select ENSP00000206765.6:n.1491+97del
ENST00000206765.10:c.1491+97del ENSP00000206765.6:n.1491+97del
ENST00000544573.5:c.165+97del ENSP00000439446.1:n.165+97del
ENST00000559136.1:c.564+97del ENSP00000453337.1:n.564+97del
NM_000359.2:c.1491+97del NP_000350.1:n.1491+97del
NM_000359.3:c.1491+97del MANE Select NP_000350.1:n.1491+97del
Search 100 bp 5'
Search 100 bp 3'