Canonical Allele Identifier: CA2680962300
Gene: GTF2H5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158191927G>T , CM000668.2:g.158191927G>T GRCh38
NC_000006.11:g.158612959G>T , CM000668.1:g.158612959G>T GRCh37
NC_000006.10:g.158532947G>T NCBI36
NG_011758.1:g.28581G>T , LRG_469:g.28581G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684993.1:n.95-50G>T
ENST00000689018.1:n.41-1283G>T
ENST00000689809.1:c.36-50G>T ENSP00000510752.1:n.36-50G>T
ENST00000691867.1:c.36-50G>T ENSP00000510706.1:n.36-50G>T
ENST00000607778.2:c.36-50G>T MANE Select ENSP00000476100.1:n.36-50G>T
ENST00000648328.1:c.*1-50G>T ENSP00000497338.1:n.*1-50G>T
ENST00000607778.1:c.36-50G>T ENSP00000476100.1:n.36-50G>T
NM_207118.2:c.36-50G>T , LRG_469t1:c.36-50G>T NP_997001.1:n.36-50G>T
XM_017010862.1:c.66-50G>T XP_016866351.1:n.66-50G>T
NM_207118.3:c.36-50G>T MANE Select NP_997001.1:n.36-50G>T