Canonical Allele Identifier: CA1955551757
Gene: GTF2H1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18335911G= , CM000673.2:g.18335911G= GRCh38
NC_000011.9:g.18357458G= , CM000673.1:g.18357458G= GRCh37
NC_000011.8:g.18314034G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265963.9:c.312G= MANE Select ENSP00000265963.4:p.Lys104=
ENST00000265963.8:c.312G= ENSP00000265963.4:p.Lys104=
ENST00000418116.6:n.511G=
ENST00000453096.6:c.312G= ENSP00000393638.2:p.Lys104=
ENST00000534641.5:c.-1-2198G= ENSP00000435375.1:n.-1-2198G=
ENST00000543932.5:n.725G=
NM_001142307.1:c.312G= NP_001135779.1:p.Lys104=
NM_005316.3:c.312G= NP_005307.1:p.Lys104=
XM_006718208.2:c.312G= XP_006718271.1:p.Lys104=
XM_006718208.3:c.312G= XP_006718271.1:p.Lys104=
XM_024448457.1:c.312G= XP_024304225.1:p.Lys104=
XM_024448458.1:c.312G= XP_024304226.1:p.Lys104=
NM_005316.4:c.312G= MANE Select NP_005307.1:p.Lys104=
NM_001142307.2:c.312G= NP_001135779.1:p.Lys104=