Canonical Allele Identifier: CA2470909901
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19577740C= , CM000686.2:g.19577740C= GRCh38
NC_000024.9:g.21739626C= , CM000686.1:g.21739626C= GRCh37
NC_000024.8:g.20199014C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.200-9470C=
ENST00000686905.1:n.134-9470C=
ENST00000693214.1:n.222-9470C=
ENST00000445715.6:n.102-9470C=
ENST00000407724.7:n.171-9470C=
ENST00000445715.5:n.102-9470C=
ENST00000447202.2:n.124-9470C=
ENST00000447520.5:n.102-9470C=
ENST00000459719.6:n.222-9470C=
ENST00000538014.2:n.240+8281C=
NR_045128.1:n.126-9470C=
NR_045129.1:n.126-9470C=