Canonical Allele Identifier: CA2470910519
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589529G= , CM000686.2:g.19589529G= GRCh38
NC_000024.9:g.21751415G= , CM000686.1:g.21751415G= GRCh37
NC_000024.8:g.20210803G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.506G=
ENST00000686905.1:n.1591G=
ENST00000693214.1:n.1679G=
ENST00000445715.6:n.408G=
ENST00000407724.7:n.752G=
ENST00000445715.5:n.408G=
ENST00000447202.2:n.2443G=
ENST00000447520.5:n.408G=
ENST00000459719.6:n.1679G=
ENST00000538014.2:n.1698G=
ENST00000585549.5:n.51G=
ENST00000587095.1:n.49G=
ENST00000588613.5:n.117G=
ENST00000589075.5:n.90G=
NR_045128.1:n.432G=
NR_045129.1:n.432G=