Canonical Allele Identifier: CA520137709

Gene: TXLNGY

Linked Data

• MyVariant Identifiers: chrY:g.21751427A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589541A>C , CM000686.2:g.19589541A>C	GRCh38
NC_000024.9:g.21751427A>C , CM000686.1:g.21751427A>C	GRCh37
NC_000024.8:g.20210815A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.518A>C
ENST00000686905.1:n.1603A>C
ENST00000693214.1:n.1691A>C
ENST00000445715.6:n.420A>C
ENST00000407724.7:n.764A>C
ENST00000445715.5:n.420A>C
ENST00000447202.2:n.2455A>C
ENST00000447520.5:n.420A>C
ENST00000459719.6:n.1691A>C
ENST00000538014.2:n.1710A>C
ENST00000585549.5:n.63A>C
ENST00000587095.1:n.61A>C
ENST00000588613.5:n.129A>C
ENST00000589075.5:n.102A>C
NR_045128.1:n.444A>C
NR_045129.1:n.444A>C