Canonical Allele Identifier: CA292045280

Gene: TEX14

Linked Data

• dbSNP Id: rs412000
• gnomAD v3: 17-58631697-G-T
• gnomAD v4: 17-58631697-G-T
• MyVariant Identifiers: chr17:g.56709058G>T (hg19) ; chr17:g.58631697G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58631697G>T , CM000679.2:g.58631697G>T	GRCh38
NC_000017.10:g.56709058G>T , CM000679.1:g.56709058G>T	GRCh37
NC_000017.9:g.54064057G>T	NCBI36
NG_047169.1:g.65383C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000349033.10:c.137-1143C>A MANE Select	ENSP00000268910.8:n.137-1143C>A
ENST00000240361.12:c.137-1143C>A	ENSP00000240361.8:n.137-1143C>A
ENST00000349033.9:c.137-1143C>A	ENSP00000268910.8:n.137-1143C>A
ENST00000389934.7:c.137-1143C>A	ENSP00000374584.3:n.137-1143C>A
ENST00000582740.1:c.*57-1143C>A	ENSP00000463593.1:n.*57-1143C>A
NM_001201457.1:c.137-1143C>A	NP_001188386.1:n.137-1143C>A
NM_031272.4:c.137-1143C>A	NP_112562.3:n.137-1143C>A
NM_198393.3:c.137-1143C>A	NP_938207.2:n.137-1143C>A
XM_011525028.1:c.137-1143C>A	XP_011523330.1:n.137-1143C>A
XM_011525029.1:c.137-1143C>A	XP_011523331.1:n.137-1143C>A
XM_011525030.1:c.137-1143C>A	XP_011523332.1:n.137-1143C>A
XM_011525031.1:c.137-1143C>A	XP_011523333.1:n.137-1143C>A
XM_011525032.1:c.137-1143C>A	XP_011523334.1:n.137-1143C>A
XM_011525029.3:c.137-1143C>A	XP_011523331.1:n.137-1143C>A
XM_017024861.1:c.-861-1143C>A	XP_016880350.1:n.-861-1143C>A
NM_001201457.2:c.137-1143C>A	NP_001188386.1:n.137-1143C>A
NM_031272.5:c.137-1143C>A MANE Select	NP_112562.3:n.137-1143C>A
NM_198393.4:c.137-1143C>A	NP_938207.2:n.137-1143C>A