Canonical Allele Identifier: CA2470909233
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19568318T= , CM000686.2:g.19568318T= GRCh38
NC_000024.9:g.21730204T= , CM000686.1:g.21730204T= GRCh37
NC_000024.8:g.20189592T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000685919.1:n.967T=
ENST00000686158.1:n.199+748T=
ENST00000686905.1:n.133+836T=
ENST00000688167.1:n.967T=
ENST00000688449.1:n.480T=
ENST00000689102.1:n.488T=
ENST00000691331.1:n.488T=
ENST00000691759.1:n.480T=
ENST00000693214.1:n.221+748T=
ENST00000445715.6:n.101+836T=
ENST00000407724.7:n.170+836T=
ENST00000445715.5:n.101+836T=
ENST00000447202.2:n.123+367T=
ENST00000447520.5:n.101+836T=
ENST00000459719.6:n.221+748T=
ENST00000538014.2:n.165+367T=
NR_045128.1:n.125+836T=
NR_045129.1:n.125+836T=