Canonical Allele Identifier: CA14476802
Gene: TEX14 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12946522

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58690742T>G , CM000679.2:g.58690742T>G GRCh38
NC_000017.10:g.56768103T>G , CM000679.1:g.56768103T>G GRCh37
NC_000017.9:g.54123102T>G NCBI36
NG_023199.1:g.3141T>G , LRG_314:g.3141T>G
NG_047169.1:g.6338A>C

Transcript Alleles

HGVS Amino-acid change
NM_001201457.1:c.-2+1197A>C VV NP_001188386.1:p.=
NM_031272.4:c.-2+1197A>C VV NP_112562.3:p.=
NM_198393.3:c.-2+1197A>C VV NP_938207.2:p.=
XM_011525028.1:c.-2+1197A>C XP_011523330.1:p.=
XM_011525030.1:c.-2+1197A>C XP_011523332.1:p.=
XM_011525031.1:c.-2+1197A>C XP_011523333.1:p.=
XM_011525032.1:c.-2+1197A>C XP_011523334.1:p.=
ENST00000240361.12:c.-2+1197A>C ENSP00000240361.8:p.=
ENST00000349033.9:c.-2+1197A>C ENSP00000268910.8:p.=
ENST00000389934.7:c.-2+1197A>C ENSP00000374584.3:p.=
ENST00000582740.1:c.-2+1197A>C ENSP00000463593.1:p.=