Canonical Allele Identifier: CA400338181

Gene: TEX14

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58572089G>T , CM000679.2:g.58572089G>T	GRCh38
NC_000017.10:g.56649450G>T , CM000679.1:g.56649450G>T	GRCh37
NC_000017.9:g.54004449G>T	NCBI36
NG_047169.1:g.124991C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349033.10:c.3549C>A MANE Select	ENSP00000268910.8:p.Cys1183Ter
ENST00000240361.12:c.3687C>A	ENSP00000240361.8:p.Cys1229Ter
ENST00000349033.9:c.3549C>A	ENSP00000268910.8:p.Cys1183Ter
ENST00000389934.7:c.3669C>A	ENSP00000374584.3:p.Cys1223Ter
ENST00000581147.1:c.109C>A
ENST00000582740.1:c.*3387C>A	ENSP00000463593.1:n.*3387C>A
NM_001201457.1:c.3687C>A	NP_001188386.1:p.Cys1229Ter
NM_031272.4:c.3549C>A	NP_112562.3:p.Cys1183Ter
NM_198393.3:c.3669C>A	NP_938207.2:p.Cys1223Ter
XM_011525028.1:c.3792C>A	XP_011523330.1:p.Cys1264Ter
XM_011525029.1:c.3792C>A	XP_011523331.1:p.Cys1264Ter
XM_011525030.1:c.3792C>A	XP_011523332.1:p.Cys1264Ter
XM_011525031.1:c.3792C>A	XP_011523333.1:p.Cys1264Ter
XM_011525032.1:c.3555C>A	XP_011523334.1:p.Cys1185Ter
XM_011525033.1:c.2493C>A	XP_011523335.1:p.Cys831Ter
XM_011525029.3:c.3792C>A	XP_011523331.1:p.Cys1264Ter
XM_017024861.1:c.2493C>A	XP_016880350.1:p.Cys831Ter
NM_001201457.2:c.3687C>A	NP_001188386.1:p.Cys1229Ter
NM_031272.5:c.3549C>A MANE Select	NP_112562.3:p.Cys1183Ter
NM_198393.4:c.3669C>A	NP_938207.2:p.Cys1223Ter