Canonical Allele Identifier: CA923753898

Gene: TXLNGY

Linked Data

• dbSNP Id: rs2045134821
• gnomAD v3: Y-19589742-CTCCTT-C
• gnomAD v4: Y-19589742-CTCCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589745_19589749del , CM000686.2:g.19589745_19589749del	GRCh38
NC_000024.9:g.21751631_21751635del , CM000686.1:g.21751631_21751635del	GRCh37
NC_000024.8:g.20211019_20211023del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.589+133_589+137del
ENST00000686905.1:n.1807_1811del
ENST00000693214.1:n.1895_1899del
ENST00000445715.6:n.491+133_491+137del
ENST00000407724.7:n.835+133_835+137del
ENST00000445715.5:n.491+133_491+137del
ENST00000447202.2:n.2659_2663del
ENST00000447520.5:n.491+133_491+137del
ENST00000459719.6:n.1762+133_1762+137del
ENST00000538014.2:n.1914_1918del
ENST00000585549.5:n.134+133_134+137del
ENST00000587095.1:n.132+133_132+137del
ENST00000588613.5:n.200+133_200+137del
ENST00000589075.5:n.173+133_173+137del
NR_045128.1:n.515+133_515+137del
NR_045129.1:n.515+133_515+137del