Canonical Allele Identifier: CA519724317

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655276T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787235T>C , CM000686.2:g.2787235T>C	GRCh38
NC_000024.9:g.2655276T>C , CM000686.1:g.2655276T>C	GRCh37
NC_000024.8:g.2715276T>C	NCBI36
NG_011751.1:g.5517A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12496T>C
ENST00000679825.1:n.347T>C
ENST00000680285.1:n.320-2514T>C
ENST00000680845.1:n.165+182T>C
ENST00000681787.1:n.106+12496T>C
ENST00000681940.1:n.106+12496T>C
ENST00000383070.2:c.369A>G MANE Select	ENSP00000372547.1:p.Lys123=
ENST00000383070.1:c.369A>G	ENSP00000372547.1:p.Lys123=
NM_003140.2:c.369A>G	NP_003131.1:p.Lys123=
NM_003140.3:c.369A>G MANE Select	NP_003131.1:p.Lys123=