Canonical Allele Identifier: CA2562649994

Gene: GTF2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18335692dup , CM000673.2:g.18335692dup	GRCh38
NC_000011.9:g.18357239dup , CM000673.1:g.18357239dup	GRCh37
NC_000011.8:g.18313815dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.155-62dup MANE Select	ENSP00000265963.4:n.155-62dup
ENST00000265963.8:c.155-62dup	ENSP00000265963.4:n.155-62dup
ENST00000418116.6:n.354-62dup
ENST00000453096.6:c.155-62dup	ENSP00000393638.2:n.155-62dup
ENST00000525831.5:c.155-62dup	ENSP00000431481.1:n.155-62dup
ENST00000531757.5:n.425-62dup
ENST00000534641.5:c.-1-2417dup	ENSP00000435375.1:n.-1-2417dup
ENST00000543932.5:n.568-62dup
NM_001142307.1:c.155-62dup	NP_001135779.1:n.155-62dup
NM_005316.3:c.155-62dup	NP_005307.1:n.155-62dup
XM_006718208.2:c.155-62dup	XP_006718271.1:n.155-62dup
XM_006718208.3:c.155-62dup	XP_006718271.1:n.155-62dup
XM_024448457.1:c.155-62dup	XP_024304225.1:n.155-62dup
XM_024448458.1:c.155-62dup	XP_024304226.1:n.155-62dup
NM_005316.4:c.155-62dup MANE Select	NP_005307.1:n.155-62dup
NM_001142307.2:c.155-62dup	NP_001135779.1:n.155-62dup