Canonical Allele Identifier: CA2469659947

Gene: SRY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787139G= , CM000686.2:g.2787139G=	GRCh38
NC_000024.9:g.2655180G= , CM000686.1:g.2655180G=	GRCh37
NC_000024.8:g.2715180G=	NCBI36
NG_011751.1:g.5613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12400G=
ENST00000679825.1:n.251G=
ENST00000680285.1:n.320-2610G=
ENST00000680845.1:n.165+86G=
ENST00000681787.1:n.106+12400G=
ENST00000681940.1:n.106+12400G=
ENST00000383070.2:c.465C= MANE Select	ENSP00000372547.1:p.Ser155=
ENST00000383070.1:c.465C=	ENSP00000372547.1:p.Ser155=
NM_003140.2:c.465C=	NP_003131.1:p.Ser155=
NM_003140.3:c.465C= MANE Select	NP_003131.1:p.Ser155=