Canonical Allele Identifier: CA519724014

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655129T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787088T>G , CM000686.2:g.2787088T>G	GRCh38
NC_000024.9:g.2655129T>G , CM000686.1:g.2655129T>G	GRCh37
NC_000024.8:g.2715129T>G	NCBI36
NG_011751.1:g.5664A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+12349T>G
ENST00000679825.1:n.200T>G
ENST00000680285.1:n.320-2661T>G
ENST00000680845.1:n.165+35T>G
ENST00000681787.1:n.106+12349T>G
ENST00000681940.1:n.106+12349T>G
ENST00000383070.2:c.516A>C MANE Select	ENSP00000372547.1:p.Thr172=
ENST00000383070.1:c.516A>C	ENSP00000372547.1:p.Thr172=
NM_003140.2:c.516A>C	NP_003131.1:p.Thr172=
NM_003140.3:c.516A>C MANE Select	NP_003131.1:p.Thr172=