Canonical Allele Identifier: CA520139202

Gene: TXLNGY

Linked Data

• MyVariant Identifiers: chrY:g.21751583A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589697A>T , CM000686.2:g.19589697A>T	GRCh38
NC_000024.9:g.21751583A>T , CM000686.1:g.21751583A>T	GRCh37
NC_000024.8:g.20210971A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.589+85A>T
ENST00000686905.1:n.1759A>T
ENST00000693214.1:n.1847A>T
ENST00000445715.6:n.491+85A>T
ENST00000407724.7:n.835+85A>T
ENST00000445715.5:n.491+85A>T
ENST00000447202.2:n.2611A>T
ENST00000447520.5:n.491+85A>T
ENST00000459719.6:n.1762+85A>T
ENST00000538014.2:n.1866A>T
ENST00000585549.5:n.134+85A>T
ENST00000587095.1:n.132+85A>T
ENST00000588613.5:n.200+85A>T
ENST00000589075.5:n.173+85A>T
NR_045128.1:n.515+85A>T
NR_045129.1:n.515+85A>T