Canonical Allele Identifier: CA2470909333
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19570265_19570266delinsTG , CM000686.2:g.19570265_19570266delinsTG GRCh38
NC_000024.9:g.21732151_21732152delinsTG , CM000686.1:g.21732151_21732152delinsTG GRCh37
NC_000024.8:g.20191539_20191540delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.199+2695_199+2696delinsTG
ENST00000686905.1:n.133+2783_133+2784delinsTG
ENST00000693214.1:n.221+2695_221+2696delinsTG
ENST00000445715.6:n.101+2783_101+2784delinsTG
ENST00000407724.7:n.170+2783_170+2784delinsTG
ENST00000445715.5:n.101+2783_101+2784delinsTG
ENST00000447202.2:n.123+2314_123+2315delinsTG
ENST00000447520.5:n.101+2783_101+2784delinsTG
ENST00000459719.6:n.221+2695_221+2696delinsTG
ENST00000538014.2:n.240+806_240+807delinsTG
NR_045128.1:n.125+2783_125+2784delinsTG
NR_045129.1:n.125+2783_125+2784delinsTG