Canonical Allele Identifier: CA1955551681

Gene: GTF2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18335689C= , CM000673.2:g.18335689C=	GRCh38
NC_000011.9:g.18357236C= , CM000673.1:g.18357236C=	GRCh37
NC_000011.8:g.18313812C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.155-65C= MANE Select	ENSP00000265963.4:n.155-65C=
ENST00000265963.8:c.155-65C=	ENSP00000265963.4:n.155-65C=
ENST00000418116.6:n.354-65C=
ENST00000453096.6:c.155-65C=	ENSP00000393638.2:n.155-65C=
ENST00000525831.5:c.155-65C=	ENSP00000431481.1:n.155-65C=
ENST00000531757.5:n.425-65C=
ENST00000534641.5:c.-1-2420C=	ENSP00000435375.1:n.-1-2420C=
ENST00000543932.5:n.568-65C=
NM_001142307.1:c.155-65C=	NP_001135779.1:n.155-65C=
NM_005316.3:c.155-65C=	NP_005307.1:n.155-65C=
XM_006718208.2:c.155-65C=	XP_006718271.1:n.155-65C=
XM_006718208.3:c.155-65C=	XP_006718271.1:n.155-65C=
XM_024448457.1:c.155-65C=	XP_024304225.1:n.155-65C=
XM_024448458.1:c.155-65C=	XP_024304226.1:n.155-65C=
NM_005316.4:c.155-65C= MANE Select	NP_005307.1:n.155-65C=
NM_001142307.2:c.155-65C=	NP_001135779.1:n.155-65C=