Canonical Allele Identifier: CA379517740

Gene: GTF2H1

Linked Data

• MyVariant Identifiers: chr11:g.18357415A>T (hg19) ; chr11:g.18335868A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18335868A>T , CM000673.2:g.18335868A>T	GRCh38
NC_000011.9:g.18357415A>T , CM000673.1:g.18357415A>T	GRCh37
NC_000011.8:g.18313991A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.269A>T MANE Select	ENSP00000265963.4:p.Asp90Val
ENST00000265963.8:c.269A>T	ENSP00000265963.4:p.Asp90Val
ENST00000418116.6:n.468A>T
ENST00000453096.6:c.269A>T	ENSP00000393638.2:p.Asp90Val
ENST00000525831.5:c.269A>T	ENSP00000431481.1:p.Asp90Val
ENST00000531757.5:n.539A>T
ENST00000534641.5:c.-1-2241A>T	ENSP00000435375.1:n.-1-2241A>T
ENST00000543932.5:n.682A>T
NM_001142307.1:c.269A>T	NP_001135779.1:p.Asp90Val
NM_005316.3:c.269A>T	NP_005307.1:p.Asp90Val
XM_006718208.2:c.269A>T	XP_006718271.1:p.Asp90Val
XM_006718208.3:c.269A>T	XP_006718271.1:p.Asp90Val
XM_024448457.1:c.269A>T	XP_024304225.1:p.Asp90Val
XM_024448458.1:c.269A>T	XP_024304226.1:p.Asp90Val
NM_005316.4:c.269A>T MANE Select	NP_005307.1:p.Asp90Val
NM_001142307.2:c.269A>T	NP_001135779.1:p.Asp90Val