Canonical Allele Identifier: CA2123832080
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24255891_24255892delinsAC , CM000676.2:g.24255891_24255892delinsAC GRCh38
NC_000014.8:g.24725097_24725098delinsAC , CM000676.1:g.24725097_24725098delinsAC GRCh37
NC_000014.7:g.23794937_23794938delinsAC NCBI36
NG_007150.1:g.12275_12276delinsGT
NG_007150.2:g.12275_12276delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1491+97_1491+98delinsGT MANE Select ENSP00000206765.6:n.1491+97_1491+98delinsGT
ENST00000206765.10:c.1491+97_1491+98delinsGT ENSP00000206765.6:n.1491+97_1491+98delinsGT
ENST00000544573.5:c.165+97_165+98delinsGT ENSP00000439446.1:n.165+97_165+98delinsGT
ENST00000559136.1:c.564+97_564+98delinsGT ENSP00000453337.1:n.564+97_564+98delinsGT
NM_000359.2:c.1491+97_1491+98delinsGT NP_000350.1:n.1491+97_1491+98delinsGT
NM_000359.3:c.1491+97_1491+98delinsGT MANE Select NP_000350.1:n.1491+97_1491+98delinsGT