Canonical Allele Identifier: CA257893616
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs3832938
gnomAD v2: 14-24725078-CTGACTTGTATAATGAG-C
gnomAD v3: 14-24255872-CTGACTTGTATAATGAG-C
gnomAD v4: 14-24255872-CTGACTTGTATAATGAG-C
MyVariant Identifiers: chr14:g.24725079_24725094del (hg19) chr14:g.24255873_24255888del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24255880_24255895del , CM000676.2:g.24255880_24255895del GRCh38
NC_000014.8:g.24725086_24725101del , CM000676.1:g.24725086_24725101del GRCh37
NC_000014.7:g.23794926_23794941del NCBI36
NG_007150.1:g.12279_12294del
NG_007150.2:g.12279_12294del

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1491+101_1491+116del MANE Select ENSP00000206765.6:n.1491+101_1491+116del
ENST00000206765.10:c.1491+101_1491+116del ENSP00000206765.6:n.1491+101_1491+116del
ENST00000544573.5:c.165+101_165+116del ENSP00000439446.1:n.165+101_165+116del
ENST00000559136.1:c.564+101_564+116del ENSP00000453337.1:n.564+101_564+116del
NM_000359.2:c.1491+101_1491+116del NP_000350.1:n.1491+101_1491+116del
NM_000359.3:c.1491+101_1491+116del MANE Select NP_000350.1:n.1491+101_1491+116del
Search 100 bp 5'
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