Canonical Allele Identifier: CA2728906007
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs3832938

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24255880_24255895dup , CM000676.2:g.24255880_24255895dup GRCh38
NC_000014.8:g.24725086_24725101dup , CM000676.1:g.24725086_24725101dup GRCh37
NC_000014.7:g.23794926_23794941dup NCBI36
NG_007150.1:g.12279_12294dup
NG_007150.2:g.12279_12294dup

Transcript Alleles

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