Canonical Allele Identifier: CA2680962293
Gene: GTF2H5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158191909A>T , CM000668.2:g.158191909A>T GRCh38
NC_000006.11:g.158612941A>T , CM000668.1:g.158612941A>T GRCh37
NC_000006.10:g.158532929A>T NCBI36
NG_011758.1:g.28563A>T , LRG_469:g.28563A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684993.1:n.95-68A>T
ENST00000689018.1:n.41-1301A>T
ENST00000689809.1:c.36-68A>T ENSP00000510752.1:n.36-68A>T
ENST00000691867.1:c.36-68A>T ENSP00000510706.1:n.36-68A>T
ENST00000607778.2:c.36-68A>T MANE Select ENSP00000476100.1:n.36-68A>T
ENST00000648328.1:c.*1-68A>T ENSP00000497338.1:n.*1-68A>T
ENST00000607778.1:c.36-68A>T ENSP00000476100.1:n.36-68A>T
NM_207118.2:c.36-68A>T , LRG_469t1:c.36-68A>T NP_997001.1:n.36-68A>T
XM_017010862.1:c.66-68A>T XP_016866351.1:n.66-68A>T
NM_207118.3:c.36-68A>T MANE Select NP_997001.1:n.36-68A>T