Canonical Allele Identifier: CA337399755

Gene: TXLNGY

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19579817G>C , CM000686.2:g.19579817G>C	GRCh38
NC_000024.9:g.21741703G>C , CM000686.1:g.21741703G>C	GRCh37
NC_000024.8:g.20201091G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.200-7393G>C
ENST00000686905.1:n.134-7393G>C
ENST00000693214.1:n.222-7393G>C
ENST00000445715.6:n.102-7393G>C
ENST00000407724.7:n.171-7393G>C
ENST00000445715.5:n.102-7393G>C
ENST00000447202.2:n.124-7393G>C
ENST00000447520.5:n.102-7393G>C
ENST00000459719.6:n.222-7393G>C
ENST00000538014.2:n.241-7393G>C
NR_045128.1:n.126-7393G>C
NR_045129.1:n.126-7393G>C