Canonical Allele Identifier: CA2470909231
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19568301G= , CM000686.2:g.19568301G= GRCh38
NC_000024.9:g.21730187G= , CM000686.1:g.21730187G= GRCh37
NC_000024.8:g.20189575G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000685919.1:n.950G=
ENST00000686158.1:n.199+731G=
ENST00000686905.1:n.133+819G=
ENST00000688167.1:n.950G=
ENST00000688449.1:n.463G=
ENST00000689102.1:n.471G=
ENST00000691331.1:n.471G=
ENST00000691759.1:n.463G=
ENST00000693214.1:n.221+731G=
ENST00000445715.6:n.101+819G=
ENST00000407724.7:n.170+819G=
ENST00000445715.5:n.101+819G=
ENST00000447202.2:n.123+350G=
ENST00000447520.5:n.101+819G=
ENST00000459719.6:n.221+731G=
ENST00000538014.2:n.165+350G=
NR_045128.1:n.125+819G=
NR_045129.1:n.125+819G=