Canonical Allele Identifier: CA520137060

Gene: TXLNGY

Linked Data

• MyVariant Identifiers: chrY:g.21751355G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589469G>T , CM000686.2:g.19589469G>T	GRCh38
NC_000024.9:g.21751355G>T , CM000686.1:g.21751355G>T	GRCh37
NC_000024.8:g.20210743G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000686158.1:n.498-52G>T
ENST00000686905.1:n.1531G>T
ENST00000693214.1:n.1619G>T
ENST00000445715.6:n.400-52G>T
ENST00000407724.7:n.750-58G>T
ENST00000445715.5:n.400-52G>T
ENST00000447202.2:n.2383G>T
ENST00000447520.5:n.400-52G>T
ENST00000459719.6:n.1619G>T
ENST00000538014.2:n.1638G>T
ENST00000585549.5:n.43-52G>T
ENST00000587095.1:n.41-52G>T
ENST00000588613.5:n.109-52G>T
ENST00000589075.5:n.82-52G>T
NR_045128.1:n.424-52G>T
NR_045129.1:n.424-52G>T