Canonical Allele Identifier: CA923765189
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs2045117758

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19570509del , CM000686.2:g.19570509del GRCh38
NC_000024.9:g.21732395del , CM000686.1:g.21732395del GRCh37
NC_000024.8:g.20191783del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.199+2939del
ENST00000686905.1:n.133+3027del
ENST00000693214.1:n.221+2939del
ENST00000445715.6:n.101+3027del
ENST00000407724.7:n.170+3027del
ENST00000445715.5:n.101+3027del
ENST00000447202.2:n.123+2558del
ENST00000447520.5:n.101+3027del
ENST00000459719.6:n.221+2939del
ENST00000538014.2:n.240+1050del
NR_045128.1:n.125+3027del
NR_045129.1:n.125+3027del