Canonical Allele Identifier: CA519724077

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655387T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787346T>A , CM000686.2:g.2787346T>A	GRCh38
NC_000024.9:g.2655387T>A , CM000686.1:g.2655387T>A	GRCh37
NC_000024.8:g.2715387T>A	NCBI36
NG_011751.1:g.5406A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12607T>A
ENST00000679825.1:n.458T>A
ENST00000680285.1:n.320-2403T>A
ENST00000680845.1:n.166-134T>A
ENST00000681787.1:n.106+12607T>A
ENST00000681940.1:n.106+12607T>A
ENST00000383070.2:c.258A>T MANE Select	ENSP00000372547.1:p.Arg86=
ENST00000383070.1:c.258A>T	ENSP00000372547.1:p.Arg86=
NM_003140.2:c.258A>T	NP_003131.1:p.Arg86=
NM_003140.3:c.258A>T MANE Select	NP_003131.1:p.Arg86=