Canonical Allele Identifier: CA1955551739
Gene: GTF2H1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18335839C= , CM000673.2:g.18335839C= GRCh38
NC_000011.9:g.18357386C= , CM000673.1:g.18357386C= GRCh37
NC_000011.8:g.18313962C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265963.9:c.240C= MANE Select ENSP00000265963.4:p.Ser80=
ENST00000265963.8:c.240C= ENSP00000265963.4:p.Ser80=
ENST00000418116.6:n.439C=
ENST00000453096.6:c.240C= ENSP00000393638.2:p.Ser80=
ENST00000525831.5:c.240C= ENSP00000431481.1:p.Ser80=
ENST00000531757.5:n.510C=
ENST00000534641.5:c.-1-2270C= ENSP00000435375.1:n.-1-2270C=
ENST00000543932.5:n.653C=
NM_001142307.1:c.240C= NP_001135779.1:p.Ser80=
NM_005316.3:c.240C= NP_005307.1:p.Ser80=
XM_006718208.2:c.240C= XP_006718271.1:p.Ser80=
XM_006718208.3:c.240C= XP_006718271.1:p.Ser80=
XM_024448457.1:c.240C= XP_024304225.1:p.Ser80=
XM_024448458.1:c.240C= XP_024304226.1:p.Ser80=
NM_005316.4:c.240C= MANE Select NP_005307.1:p.Ser80=
NM_001142307.2:c.240C= NP_001135779.1:p.Ser80=