Canonical Allele Identifier: CA379517752

Gene: GTF2H1

Linked Data

• MyVariant Identifiers: chr11:g.18357418C>G (hg19) ; chr11:g.18335871C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18335871C>G , CM000673.2:g.18335871C>G	GRCh38
NC_000011.9:g.18357418C>G , CM000673.1:g.18357418C>G	GRCh37
NC_000011.8:g.18313994C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.272C>G MANE Select	ENSP00000265963.4:p.Ala91Gly
ENST00000265963.8:c.272C>G	ENSP00000265963.4:p.Ala91Gly
ENST00000418116.6:n.471C>G
ENST00000453096.6:c.272C>G	ENSP00000393638.2:p.Ala91Gly
ENST00000525831.5:c.272C>G	ENSP00000431481.1:p.Ala91Gly
ENST00000531757.5:n.542C>G
ENST00000534641.5:c.-1-2238C>G	ENSP00000435375.1:n.-1-2238C>G
ENST00000543932.5:n.685C>G
NM_001142307.1:c.272C>G	NP_001135779.1:p.Ala91Gly
NM_005316.3:c.272C>G	NP_005307.1:p.Ala91Gly
XM_006718208.2:c.272C>G	XP_006718271.1:p.Ala91Gly
XM_006718208.3:c.272C>G	XP_006718271.1:p.Ala91Gly
XM_024448457.1:c.272C>G	XP_024304225.1:p.Ala91Gly
XM_024448458.1:c.272C>G	XP_024304226.1:p.Ala91Gly
NM_005316.4:c.272C>G MANE Select	NP_005307.1:p.Ala91Gly
NM_001142307.2:c.272C>G	NP_001135779.1:p.Ala91Gly