Canonical Allele Identifier: CA337399413
Gene: TXLNGY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19571277_19571278insAA , CM000686.2:g.19571277_19571278insAA GRCh38
NC_000024.9:g.21733163_21733164insAA , CM000686.1:g.21733163_21733164insAA GRCh37
NC_000024.8:g.20192551_20192552insAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.199+3707_199+3708insAA
ENST00000686905.1:n.133+3795_133+3796insAA
ENST00000693214.1:n.221+3707_221+3708insAA
ENST00000445715.6:n.101+3795_101+3796insAA
ENST00000407724.7:n.170+3795_170+3796insAA
ENST00000445715.5:n.101+3795_101+3796insAA
ENST00000447202.2:n.123+3326_123+3327insAA
ENST00000447520.5:n.101+3795_101+3796insAA
ENST00000459719.6:n.221+3707_221+3708insAA
ENST00000538014.2:n.240+1818_240+1819insAA
NR_045128.1:n.125+3795_125+3796insAA
NR_045129.1:n.125+3795_125+3796insAA
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