Canonical Allele Identifier: CA2003585742
Gene: TREH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118659706T= , CM000673.2:g.118659706T= GRCh38
NC_000011.9:g.118530415T= , CM000673.1:g.118530415T= GRCh37
NC_000011.8:g.118035625T= NCBI36
NG_023321.1:g.24967A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264029.9:c.1320+41A= MANE Select ENSP00000264029.5:n.1320+41A=
ENST00000264029.8:c.1320+41A= ENSP00000264029.5:n.1320+41A=
ENST00000397925.2:c.1227+41A= ENSP00000381020.2:n.1227+41A=
ENST00000613915.4:c.*1097+41A= ENSP00000477923.1:n.*1097+41A=
NM_001301065.1:c.1227+41A= NP_001287994.1:n.1227+41A=
NM_007180.2:c.1320+41A= NP_009111.2:n.1320+41A=
XM_011542564.1:c.897+41A= XP_011540866.1:n.897+41A=
NM_001301065.2:c.1227+41A= NP_001287994.1:n.1227+41A=
NM_007180.3:c.1320+41A= MANE Select NP_009111.2:n.1320+41A=
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