Canonical Allele Identifier: CA3047986354
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19570429dup , CM000686.2:g.19570429dup GRCh38
NC_000024.9:g.21732315dup , CM000686.1:g.21732315dup GRCh37
NC_000024.8:g.20191703dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.199+2859dup
ENST00000686905.1:n.133+2947dup
ENST00000693214.1:n.221+2859dup
ENST00000445715.6:n.101+2947dup
ENST00000407724.7:n.170+2947dup
ENST00000445715.5:n.101+2947dup
ENST00000447202.2:n.123+2478dup
ENST00000447520.5:n.101+2947dup
ENST00000459719.6:n.221+2859dup
ENST00000538014.2:n.240+970dup
NR_045128.1:n.125+2947dup
NR_045129.1:n.125+2947dup