Canonical Allele Identifier: CA1955551804

Gene: GTF2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18336042_18336043delinsGT , CM000673.2:g.18336042_18336043delinsGT	GRCh38
NC_000011.9:g.18357589_18357590delinsGT , CM000673.1:g.18357589_18357590delinsGT	GRCh37
NC_000011.8:g.18314165_18314166delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.347+96_347+97delinsGT MANE Select	ENSP00000265963.4:n.347+96_347+97delinsGT
ENST00000265963.8:c.347+96_347+97delinsGT	ENSP00000265963.4:n.347+96_347+97delinsGT
ENST00000418116.6:n.546+96_546+97delinsGT
ENST00000453096.6:c.347+96_347+97delinsGT	ENSP00000393638.2:n.347+96_347+97delinsGT
ENST00000534641.5:c.-1-2067_-1-2066delinsGT	ENSP00000435375.1:n.-1-2067_-1-2066delinsGT
ENST00000543932.5:n.760+96_760+97delinsGT
NM_001142307.1:c.347+96_347+97delinsGT	NP_001135779.1:n.347+96_347+97delinsGT
NM_005316.3:c.347+96_347+97delinsGT	NP_005307.1:n.347+96_347+97delinsGT
XM_006718208.2:c.347+96_347+97delinsGT	XP_006718271.1:n.347+96_347+97delinsGT
XM_006718208.3:c.347+96_347+97delinsGT	XP_006718271.1:n.347+96_347+97delinsGT
XM_024448457.1:c.347+96_347+97delinsGT	XP_024304225.1:n.347+96_347+97delinsGT
XM_024448458.1:c.347+96_347+97delinsGT	XP_024304226.1:n.347+96_347+97delinsGT
NM_005316.4:c.347+96_347+97delinsGT MANE Select	NP_005307.1:n.347+96_347+97delinsGT
NM_001142307.2:c.347+96_347+97delinsGT	NP_001135779.1:n.347+96_347+97delinsGT