Canonical Allele Identifier: CA520137159

Gene: TXLNGY

Linked Data

• MyVariant Identifiers: chrY:g.21751368C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589482C>A , CM000686.2:g.19589482C>A	GRCh38
NC_000024.9:g.21751368C>A , CM000686.1:g.21751368C>A	GRCh37
NC_000024.8:g.20210756C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.498-39C>A
ENST00000686905.1:n.1544C>A
ENST00000693214.1:n.1632C>A
ENST00000445715.6:n.400-39C>A
ENST00000407724.7:n.750-45C>A
ENST00000445715.5:n.400-39C>A
ENST00000447202.2:n.2396C>A
ENST00000447520.5:n.400-39C>A
ENST00000459719.6:n.1632C>A
ENST00000538014.2:n.1651C>A
ENST00000585549.5:n.43-39C>A
ENST00000587095.1:n.41-39C>A
ENST00000588613.5:n.109-39C>A
ENST00000589075.5:n.82-39C>A
NR_045128.1:n.424-39C>A
NR_045129.1:n.424-39C>A