Canonical Allele Identifier: CA379517543

Gene: GTF2H1

Linked Data

• MyVariant Identifiers: chr11:g.18357358C>T (hg19) ; chr11:g.18335811C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18335811C>T , CM000673.2:g.18335811C>T	GRCh38
NC_000011.9:g.18357358C>T , CM000673.1:g.18357358C>T	GRCh37
NC_000011.8:g.18313934C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.212C>T MANE Select	ENSP00000265963.4:p.Ala71Val
ENST00000265963.8:c.212C>T	ENSP00000265963.4:p.Ala71Val
ENST00000418116.6:n.411C>T
ENST00000453096.6:c.212C>T	ENSP00000393638.2:p.Ala71Val
ENST00000525831.5:c.212C>T	ENSP00000431481.1:p.Ala71Val
ENST00000531757.5:n.482C>T
ENST00000534641.5:c.-1-2298C>T	ENSP00000435375.1:n.-1-2298C>T
ENST00000543932.5:n.625C>T
NM_001142307.1:c.212C>T	NP_001135779.1:p.Ala71Val
NM_005316.3:c.212C>T	NP_005307.1:p.Ala71Val
XM_006718208.2:c.212C>T	XP_006718271.1:p.Ala71Val
XM_006718208.3:c.212C>T	XP_006718271.1:p.Ala71Val
XM_024448457.1:c.212C>T	XP_024304225.1:p.Ala71Val
XM_024448458.1:c.212C>T	XP_024304226.1:p.Ala71Val
NM_005316.4:c.212C>T MANE Select	NP_005307.1:p.Ala71Val
NM_001142307.2:c.212C>T	NP_001135779.1:p.Ala71Val