Canonical Allele Identifier: CA520136869

Gene: TXLNGY

Linked Data

• MyVariant Identifiers: chrY:g.21751338C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589452C>T , CM000686.2:g.19589452C>T	GRCh38
NC_000024.9:g.21751338C>T , CM000686.1:g.21751338C>T	GRCh37
NC_000024.8:g.20210726C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.498-69C>T
ENST00000686905.1:n.1514C>T
ENST00000693214.1:n.1602C>T
ENST00000445715.6:n.400-69C>T
ENST00000407724.7:n.750-75C>T
ENST00000445715.5:n.400-69C>T
ENST00000447202.2:n.2366C>T
ENST00000447520.5:n.400-69C>T
ENST00000459719.6:n.1602C>T
ENST00000538014.2:n.1621C>T
ENST00000585549.5:n.43-69C>T
ENST00000587095.1:n.41-69C>T
ENST00000588613.5:n.109-69C>T
ENST00000589075.5:n.82-69C>T
NR_045128.1:n.424-69C>T
NR_045129.1:n.424-69C>T