Canonical Allele Identifier: CA961133276
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs1355342948

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24256350_24256352dup , CM000676.2:g.24256350_24256352dup GRCh38
NC_000014.8:g.24725556_24725558dup , CM000676.1:g.24725556_24725558dup GRCh37
NC_000014.7:g.23795396_23795398dup NCBI36
NG_007150.1:g.11817_11819dup
NG_007150.2:g.11817_11819dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1403-273_1403-271dup MANE Select ENSP00000206765.6:n.1403-273_1403-271dup
ENST00000206765.10:c.1403-273_1403-271dup ENSP00000206765.6:n.1403-273_1403-271dup
ENST00000544573.5:c.77-273_77-271dup ENSP00000439446.1:n.77-273_77-271dup
ENST00000559136.1:c.476-273_476-271dup ENSP00000453337.1:n.476-273_476-271dup
NM_000359.2:c.1403-273_1403-271dup NP_000350.1:n.1403-273_1403-271dup
NM_000359.3:c.1403-273_1403-271dup MANE Select NP_000350.1:n.1403-273_1403-271dup