Canonical Allele Identifier: CA519724288

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655257G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787216G>T , CM000686.2:g.2787216G>T	GRCh38
NC_000024.9:g.2655257G>T , CM000686.1:g.2655257G>T	GRCh37
NC_000024.8:g.2715257G>T	NCBI36
NG_011751.1:g.5536C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12477G>T
ENST00000679825.1:n.328G>T
ENST00000680285.1:n.320-2533G>T
ENST00000680845.1:n.165+163G>T
ENST00000681787.1:n.106+12477G>T
ENST00000681940.1:n.106+12477G>T
ENST00000383070.2:c.388C>A MANE Select	ENSP00000372547.1:p.Arg130=
ENST00000383070.1:c.388C>A	ENSP00000372547.1:p.Arg130=
NM_003140.2:c.388C>A	NP_003131.1:p.Arg130=
NM_003140.3:c.388C>A MANE Select	NP_003131.1:p.Arg130=