Canonical Allele Identifier: CA923764323
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs2045116265

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19568482dup , CM000686.2:g.19568482dup GRCh38
NC_000024.9:g.21730368dup , CM000686.1:g.21730368dup GRCh37
NC_000024.8:g.20189756dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.199+912dup
ENST00000686905.1:n.133+1000dup
ENST00000693214.1:n.221+912dup
ENST00000445715.6:n.101+1000dup
ENST00000407724.7:n.170+1000dup
ENST00000445715.5:n.101+1000dup
ENST00000447202.2:n.123+531dup
ENST00000447520.5:n.101+1000dup
ENST00000459719.6:n.221+912dup
ENST00000538014.2:n.165+531dup
NR_045128.1:n.125+1000dup
NR_045129.1:n.125+1000dup