Canonical Allele Identifier: CA2469659985

Gene: SRY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787412C= , CM000686.2:g.2787412C=	GRCh38
NC_000024.9:g.2655453C= , CM000686.1:g.2655453C=	GRCh37
NC_000024.8:g.2715453C=	NCBI36
NG_011751.1:g.5340G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12673C=
ENST00000679825.1:n.524C=
ENST00000680285.1:n.320-2337C=
ENST00000680845.1:n.166-68C=
ENST00000681787.1:n.106+12673C=
ENST00000681940.1:n.106+12673C=
ENST00000383070.2:c.192G= MANE Select	ENSP00000372547.1:p.Met64=
ENST00000383070.1:c.192G=	ENSP00000372547.1:p.Met64=
NM_003140.2:c.192G=	NP_003131.1:p.Met64=
NM_003140.3:c.192G= MANE Select	NP_003131.1:p.Met64=