Canonical Allele Identifier: CA7976394

Gene: GTF3C1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.27494847G>A , CM000678.2:g.27494847G>A	GRCh38
NC_000016.9:g.27506168G>A , CM000678.1:g.27506168G>A	GRCh37
NC_000016.8:g.27413669G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356183.9:c.2694C>T MANE Select	ENSP00000348510.4:p.Phe898=
ENST00000356183.8:c.2694C>T	ENSP00000348510.4:p.Phe898=
ENST00000561623.5:c.2694C>T	ENSP00000455417.1:p.Phe898=
ENST00000569653.1:c.96+6460C>T
NM_001286242.1:c.2694C>T	NP_001273171.1:p.Phe898=
NM_001520.3:c.2694C>T	NP_001511.2:p.Phe898=
XM_011545813.1:c.2694C>T	XP_011544115.1:p.Phe898=
XM_011545814.1:c.2694C>T	XP_011544116.1:p.Phe898=
XM_011545815.1:c.2694C>T	XP_011544117.1:p.Phe898=
XM_017023188.2:c.2694C>T	XP_016878677.1:p.Phe898=
NM_001520.4:c.2694C>T MANE Select	NP_001511.2:p.Phe898=
NM_001286242.2:c.2694C>T	NP_001273171.1:p.Phe898=