Canonical Allele Identifier: CA2800897267
Gene: TGM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24256237_24256238insAGAA , CM000676.2:g.24256237_24256238insAGAA GRCh38
NC_000014.8:g.24725443_24725444insAGAA , CM000676.1:g.24725443_24725444insAGAA GRCh37
NC_000014.7:g.23795283_23795284insAGAA NCBI36
NG_007150.1:g.11929_11930insTTCT
NG_007150.2:g.11929_11930insTTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1403-161_1403-160insTTCT MANE Select ENSP00000206765.6:n.1403-161_1403-160insTTCT
ENST00000206765.10:c.1403-161_1403-160insTTCT ENSP00000206765.6:n.1403-161_1403-160insTTCT
ENST00000544573.5:c.77-161_77-160insTTCT ENSP00000439446.1:n.77-161_77-160insTTCT
ENST00000559136.1:c.476-161_476-160insTTCT ENSP00000453337.1:n.476-161_476-160insTTCT
NM_000359.2:c.1403-161_1403-160insTTCT NP_000350.1:n.1403-161_1403-160insTTCT
NM_000359.3:c.1403-161_1403-160insTTCT MANE Select NP_000350.1:n.1403-161_1403-160insTTCT