Canonical Allele Identifier: CA2555032761

Gene: SRY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787355_2787356insA , CM000686.2:g.2787355_2787356insA	GRCh38
NC_000024.9:g.2655396_2655397insA , CM000686.1:g.2655396_2655397insA	GRCh37
NC_000024.8:g.2715396_2715397insA	NCBI36
NG_011751.1:g.5396_5397insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12616_106+12617insA
ENST00000679825.1:n.467_468insA
ENST00000680285.1:n.320-2394_320-2393insA
ENST00000680845.1:n.166-125_166-124insA
ENST00000681787.1:n.106+12616_106+12617insA
ENST00000681940.1:n.106+12616_106+12617insA
ENST00000383070.2:c.248_249insT MANE Select	ENSP00000372547.1:p.Arg84GlnfsTer20
ENST00000383070.1:c.248_249insT	ENSP00000372547.1:p.Arg84GlnfsTer20
NM_003140.2:c.248_249insT	NP_003131.1:p.Arg84GlnfsTer20
NM_003140.3:c.248_249insT MANE Select	NP_003131.1:p.Arg84GlnfsTer20