Canonical Allele Identifier: CA1955551748

Gene: GTF2H1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18335872A= , CM000673.2:g.18335872A=	GRCh38
NC_000011.9:g.18357419A= , CM000673.1:g.18357419A=	GRCh37
NC_000011.8:g.18313995A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.273A= MANE Select	ENSP00000265963.4:p.Ala91=
ENST00000265963.8:c.273A=	ENSP00000265963.4:p.Ala91=
ENST00000418116.6:n.472A=
ENST00000453096.6:c.273A=	ENSP00000393638.2:p.Ala91=
ENST00000525831.5:c.273A=	ENSP00000431481.1:p.Ala91=
ENST00000531757.5:n.543A=
ENST00000534641.5:c.-1-2237A=	ENSP00000435375.1:n.-1-2237A=
ENST00000543932.5:n.686A=
NM_001142307.1:c.273A=	NP_001135779.1:p.Ala91=
NM_005316.3:c.273A=	NP_005307.1:p.Ala91=
XM_006718208.2:c.273A=	XP_006718271.1:p.Ala91=
XM_006718208.3:c.273A=	XP_006718271.1:p.Ala91=
XM_024448457.1:c.273A=	XP_024304225.1:p.Ala91=
XM_024448458.1:c.273A=	XP_024304226.1:p.Ala91=
NM_005316.4:c.273A= MANE Select	NP_005307.1:p.Ala91=
NM_001142307.2:c.273A=	NP_001135779.1:p.Ala91=