Canonical Allele Identifier: CA923766469
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs2045120019

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19574392del , CM000686.2:g.19574392del GRCh38
NC_000024.9:g.21736278del , CM000686.1:g.21736278del GRCh37
NC_000024.8:g.20195666del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.199+6822del
ENST00000686905.1:n.133+6910del
ENST00000693214.1:n.221+6822del
ENST00000445715.6:n.101+6910del
ENST00000407724.7:n.170+6910del
ENST00000445715.5:n.101+6910del
ENST00000447202.2:n.123+6441del
ENST00000447520.5:n.101+6910del
ENST00000459719.6:n.221+6822del
ENST00000538014.2:n.240+4933del
NR_045128.1:n.125+6910del
NR_045129.1:n.125+6910del