Canonical Allele Identifier: CA2469660002

Gene: SRY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787551C= , CM000686.2:g.2787551C=	GRCh38
NC_000024.9:g.2655592C= , CM000686.1:g.2655592C=	GRCh37
NC_000024.8:g.2715592C=	NCBI36
NG_011751.1:g.5201G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+12812C=
ENST00000679825.1:n.663C=
ENST00000680285.1:n.320-2198C=
ENST00000680845.1:n.237C=
ENST00000681787.1:n.106+12812C=
ENST00000681940.1:n.106+12812C=
ENST00000383070.2:c.53G= MANE Select	ENSP00000372547.1:p.Ser18=
ENST00000383070.1:c.53G=	ENSP00000372547.1:p.Ser18=
NM_003140.2:c.53G=	NP_003131.1:p.Ser18=
NM_003140.3:c.53G= MANE Select	NP_003131.1:p.Ser18=