Canonical Allele Identifier: CA519724537

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655365G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787324G>A , CM000686.2:g.2787324G>A	GRCh38
NC_000024.9:g.2655365G>A , CM000686.1:g.2655365G>A	GRCh37
NC_000024.8:g.2715365G>A	NCBI36
NG_011751.1:g.5428C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12585G>A
ENST00000679825.1:n.436G>A
ENST00000680285.1:n.320-2425G>A
ENST00000680845.1:n.166-156G>A
ENST00000681787.1:n.106+12585G>A
ENST00000681940.1:n.106+12585G>A
ENST00000383070.2:c.280C>T MANE Select	ENSP00000372547.1:p.Leu94=
ENST00000383070.1:c.280C>T	ENSP00000372547.1:p.Leu94=
NM_003140.2:c.280C>T	NP_003131.1:p.Leu94=
NM_003140.3:c.280C>T MANE Select	NP_003131.1:p.Leu94=