Canonical Allele Identifier: CA645586278
Gene: TGM1 HGNC NCBI

Linked Data

COSMIC: COSM133392

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24261696_24261697delinsAT , CM000676.2:g.24261696_24261697delinsAT GRCh38
NC_000014.8:g.24730902_24730903delinsAT , CM000676.1:g.24730902_24730903delinsAT GRCh37
NC_000014.7:g.23800742_23800743delinsAT NCBI36
NG_007150.1:g.6470_6471delinsAT
NG_007150.2:g.6470_6471delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000206765.11:c.506_507delinsAT MANE Select ENSP00000206765.6:p.Ile169Asn
ENST00000206765.10:c.506_507delinsAT ENSP00000206765.6:p.Ile169Asn
ENST00000544573.5:c.-29+430_-29+431delinsAT ENSP00000439446.1:n.-29+430_-29+431delins...
NM_000359.2:c.506_507delinsAT NP_000350.1:p.Ile169Asn
NM_000359.3:c.506_507delinsAT MANE Select NP_000350.1:p.Ile169Asn