Canonical Allele Identifier: CA2695237528

Gene: SRY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787360_2787361insA , CM000686.2:g.2787360_2787361insA	GRCh38
NC_000024.9:g.2655401_2655402insA , CM000686.1:g.2655401_2655402insA	GRCh37
NC_000024.8:g.2715401_2715402insA	NCBI36
NG_011751.1:g.5391_5392insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12621_106+12622insA
ENST00000679825.1:n.472_473insA
ENST00000680285.1:n.320-2389_320-2388insA
ENST00000680845.1:n.166-120_166-119insA
ENST00000681787.1:n.106+12621_106+12622insA
ENST00000681940.1:n.106+12621_106+12622insA
ENST00000383070.2:c.243_244insT MANE Select	ENSP00000372547.1:p.Asn82Ter
ENST00000383070.1:c.243_244insT	ENSP00000372547.1:p.Asn82Ter
NM_003140.2:c.243_244insT	NP_003131.1:p.Asn82Ter
NM_003140.3:c.243_244insT MANE Select	NP_003131.1:p.Asn82Ter