Canonical Allele Identifier: CA2470910535
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589658A= , CM000686.2:g.19589658A= GRCh38
NC_000024.9:g.21751544A= , CM000686.1:g.21751544A= GRCh37
NC_000024.8:g.20210932A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.589+46A=
ENST00000686905.1:n.1720A=
ENST00000693214.1:n.1808A=
ENST00000445715.6:n.491+46A=
ENST00000407724.7:n.835+46A=
ENST00000445715.5:n.491+46A=
ENST00000447202.2:n.2572A=
ENST00000447520.5:n.491+46A=
ENST00000459719.6:n.1762+46A=
ENST00000538014.2:n.1827A=
ENST00000585549.5:n.134+46A=
ENST00000587095.1:n.132+46A=
ENST00000588613.5:n.200+46A=
ENST00000589075.5:n.173+46A=
NR_045128.1:n.515+46A=
NR_045129.1:n.515+46A=