Canonical Allele Identifier: CA1955551758

Gene: GTF2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18335918G= , CM000673.2:g.18335918G=	GRCh38
NC_000011.9:g.18357465G= , CM000673.1:g.18357465G=	GRCh37
NC_000011.8:g.18314041G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.319G= MANE Select	ENSP00000265963.4:p.Ala107=
ENST00000265963.8:c.319G=	ENSP00000265963.4:p.Ala107=
ENST00000418116.6:n.518G=
ENST00000453096.6:c.319G=	ENSP00000393638.2:p.Ala107=
ENST00000534641.5:c.-1-2191G=	ENSP00000435375.1:n.-1-2191G=
ENST00000543932.5:n.732G=
NM_001142307.1:c.319G=	NP_001135779.1:p.Ala107=
NM_005316.3:c.319G=	NP_005307.1:p.Ala107=
XM_006718208.2:c.319G=	XP_006718271.1:p.Ala107=
XM_006718208.3:c.319G=	XP_006718271.1:p.Ala107=
XM_024448457.1:c.319G=	XP_024304225.1:p.Ala107=
XM_024448458.1:c.319G=	XP_024304226.1:p.Ala107=
NM_005316.4:c.319G= MANE Select	NP_005307.1:p.Ala107=
NM_001142307.2:c.319G=	NP_001135779.1:p.Ala107=