Canonical Allele Identifier: CA1675992811
Gene: GTF2H5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158191929T= , CM000668.2:g.158191929T= GRCh38
NC_000006.11:g.158612961T= , CM000668.1:g.158612961T= GRCh37
NC_000006.10:g.158532949T= NCBI36
NG_011758.1:g.28583T= , LRG_469:g.28583T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684993.1:n.95-48T=
ENST00000689018.1:n.41-1281T=
ENST00000689809.1:c.36-48T= ENSP00000510752.1:n.36-48T=
ENST00000691867.1:c.36-48T= ENSP00000510706.1:n.36-48T=
ENST00000607778.2:c.36-48T= MANE Select ENSP00000476100.1:n.36-48T=
ENST00000648328.1:c.*1-48T= ENSP00000497338.1:n.*1-48T=
ENST00000607778.1:c.36-48T= ENSP00000476100.1:n.36-48T=
NM_207118.2:c.36-48T= , LRG_469t1:c.36-48T= NP_997001.1:n.36-48T=
XM_017010862.1:c.66-48T= XP_016866351.1:n.66-48T=
NM_207118.3:c.36-48T= MANE Select NP_997001.1:n.36-48T=