Canonical Allele Identifier: CA519724078

Gene: SRY

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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