Canonical Allele Identifier: CA923764226
Gene: TXLNGY HGNC NCBI

Linked Data

gnomAD v3: Y-19568335-A-G
gnomAD v4: Y-19568335-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19568335A>G , CM000686.2:g.19568335A>G GRCh38
NC_000024.9:g.21730221A>G , CM000686.1:g.21730221A>G GRCh37
NC_000024.8:g.20189609A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000685919.1:n.984A>G
ENST00000686158.1:n.199+765A>G
ENST00000686905.1:n.133+853A>G
ENST00000688167.1:n.984A>G
ENST00000688449.1:n.497A>G
ENST00000689102.1:n.505A>G
ENST00000691331.1:n.505A>G
ENST00000691759.1:n.497A>G
ENST00000693214.1:n.221+765A>G
ENST00000445715.6:n.101+853A>G
ENST00000407724.7:n.170+853A>G
ENST00000445715.5:n.101+853A>G
ENST00000447202.2:n.123+384A>G
ENST00000447520.5:n.101+853A>G
ENST00000459719.6:n.221+765A>G
ENST00000538014.2:n.165+384A>G
NR_045128.1:n.125+853A>G
NR_045129.1:n.125+853A>G