Canonical Allele Identifier: CA2470910538

Gene: TXLNGY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589742_19589747delinsCTCCTT , CM000686.2:g.19589742_19589747delinsCTCCTT	GRCh38
NC_000024.9:g.21751628_21751633delinsCTCCTT , CM000686.1:g.21751628_21751633delinsCTCCTT	GRCh37
NC_000024.8:g.20211016_20211021delinsCTCCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.589+130_589+135delinsCTCCTT
ENST00000686905.1:n.1804_1809delinsCTCCTT
ENST00000693214.1:n.1892_1897delinsCTCCTT
ENST00000445715.6:n.491+130_491+135delinsCTCCTT
ENST00000407724.7:n.835+130_835+135delinsCTCCTT
ENST00000445715.5:n.491+130_491+135delinsCTCCTT
ENST00000447202.2:n.2656_2661delinsCTCCTT
ENST00000447520.5:n.491+130_491+135delinsCTCCTT
ENST00000459719.6:n.1762+130_1762+135delinsCTCCTT
ENST00000538014.2:n.1911_1916delinsCTCCTT
ENST00000585549.5:n.134+130_134+135delinsCTCCTT
ENST00000587095.1:n.132+130_132+135delinsCTCCTT
ENST00000588613.5:n.200+130_200+135delinsCTCCTT
ENST00000589075.5:n.173+130_173+135delinsCTCCTT
NR_045128.1:n.515+130_515+135delinsCTCCTT
NR_045129.1:n.515+130_515+135delinsCTCCTT