Canonical Allele Identifier: CA1675992800
Gene: GTF2H5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158191914C= , CM000668.2:g.158191914C= GRCh38
NC_000006.11:g.158612946C= , CM000668.1:g.158612946C= GRCh37
NC_000006.10:g.158532934C= NCBI36
NG_011758.1:g.28568C= , LRG_469:g.28568C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684993.1:n.95-63C=
ENST00000689018.1:n.41-1296C=
ENST00000689809.1:c.36-63C= ENSP00000510752.1:n.36-63C=
ENST00000691867.1:c.36-63C= ENSP00000510706.1:n.36-63C=
ENST00000607778.2:c.36-63C= MANE Select ENSP00000476100.1:n.36-63C=
ENST00000648328.1:c.*1-63C= ENSP00000497338.1:n.*1-63C=
ENST00000607778.1:c.36-63C= ENSP00000476100.1:n.36-63C=
NM_207118.2:c.36-63C= , LRG_469t1:c.36-63C= NP_997001.1:n.36-63C=
XM_017010862.1:c.66-63C= XP_016866351.1:n.66-63C=
NM_207118.3:c.36-63C= MANE Select NP_997001.1:n.36-63C=
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