Canonical Allele Identifier: CA2470910522
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589554A= , CM000686.2:g.19589554A= GRCh38
NC_000024.9:g.21751440A= , CM000686.1:g.21751440A= GRCh37
NC_000024.8:g.20210828A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.531A=
ENST00000686905.1:n.1616A=
ENST00000693214.1:n.1704A=
ENST00000445715.6:n.433A=
ENST00000407724.7:n.777A=
ENST00000445715.5:n.433A=
ENST00000447202.2:n.2468A=
ENST00000447520.5:n.433A=
ENST00000459719.6:n.1704A=
ENST00000538014.2:n.1723A=
ENST00000585549.5:n.76A=
ENST00000587095.1:n.74A=
ENST00000588613.5:n.142A=
ENST00000589075.5:n.115A=
NR_045128.1:n.457A=
NR_045129.1:n.457A=