Canonical Allele Identifier: CA519429429

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655072T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787031T>A , CM000686.2:g.2787031T>A	GRCh38
NC_000024.9:g.2655072T>A , CM000686.1:g.2655072T>A	GRCh37
NC_000024.8:g.2715072T>A	NCBI36
NG_011751.1:g.5721A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+12292T>A
ENST00000679825.1:n.143T>A
ENST00000680285.1:n.320-2718T>A
ENST00000680845.1:n.143T>A
ENST00000681787.1:n.106+12292T>A
ENST00000681940.1:n.106+12292T>A
ENST00000383070.2:c.573A>T MANE Select	ENSP00000372547.1:p.Ser191=
ENST00000383070.1:c.573A>T	ENSP00000372547.1:p.Ser191=
NM_003140.2:c.573A>T	NP_003131.1:p.Ser191=
NM_003140.3:c.573A>T MANE Select	NP_003131.1:p.Ser191=