Canonical Allele Identifier: CA2533501956
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19570179_19570378del , CM000686.2:g.19570179_19570378del GRCh38
NC_000024.9:g.21732065_21732264del , CM000686.1:g.21732065_21732264del GRCh37
NC_000024.8:g.20191453_20191652del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.199+2609_199+2808del
ENST00000686905.1:n.133+2697_133+2896del
ENST00000693214.1:n.221+2609_221+2808del
ENST00000445715.6:n.101+2697_101+2896del
ENST00000407724.7:n.170+2697_170+2896del
ENST00000445715.5:n.101+2697_101+2896del
ENST00000447202.2:n.123+2228_123+2427del
ENST00000447520.5:n.101+2697_101+2896del
ENST00000459719.6:n.221+2609_221+2808del
ENST00000538014.2:n.240+720_240+919del
NR_045128.1:n.125+2697_125+2896del
NR_045129.1:n.125+2697_125+2896del