Canonical Allele Identifier: CA2470909242

Gene: TXLNGY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19568474_19568478delinsCAAAA , CM000686.2:g.19568474_19568478delinsCAAAA	GRCh38
NC_000024.9:g.21730360_21730364delinsCAAAA , CM000686.1:g.21730360_21730364delinsCAAAA	GRCh37
NC_000024.8:g.20189748_20189752delinsCAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685919.1:n.1123_1127delinsCAAAA
ENST00000686158.1:n.199+904_199+908delinsCAAAA
ENST00000686905.1:n.133+992_133+996delinsCAAAA
ENST00000688167.1:n.1123_1127delinsCAAAA
ENST00000688449.1:n.636_640delinsCAAAA
ENST00000689102.1:n.644_648delinsCAAAA
ENST00000691331.1:n.644_648delinsCAAAA
ENST00000691759.1:n.636_640delinsCAAAA
ENST00000693214.1:n.221+904_221+908delinsCAAAA
ENST00000445715.6:n.101+992_101+996delinsCAAAA
ENST00000407724.7:n.170+992_170+996delinsCAAAA
ENST00000445715.5:n.101+992_101+996delinsCAAAA
ENST00000447202.2:n.123+523_123+527delinsCAAAA
ENST00000447520.5:n.101+992_101+996delinsCAAAA
ENST00000459719.6:n.221+904_221+908delinsCAAAA
ENST00000538014.2:n.165+523_165+527delinsCAAAA
NR_045128.1:n.125+992_125+996delinsCAAAA
NR_045129.1:n.125+992_125+996delinsCAAAA