Canonical Allele Identifier: CA3051355415

Gene: SRY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787298_2787299insATATTG , CM000686.2:g.2787298_2787299insATATTG	GRCh38
NC_000024.9:g.2655339_2655340insATATTG , CM000686.1:g.2655339_2655340insATATTG	GRCh37
NC_000024.8:g.2715339_2715340insATATTG	NCBI36
NG_011751.1:g.5453_5454insCAATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12559_106+12560insATATTG
ENST00000679825.1:n.410_411insATATTG
ENST00000680285.1:n.320-2451_320-2450insATATTG
ENST00000680845.1:n.166-182_166-181insATATTG
ENST00000681787.1:n.106+12559_106+12560insATATTG
ENST00000681940.1:n.106+12559_106+12560insATATTG
ENST00000383070.2:c.305_306insCAATAT MANE Select	ENSP00000372547.1:p.Thr102_Glu103insAsnIle
ENST00000383070.1:c.305_306insCAATAT	ENSP00000372547.1:p.Thr102_Glu103insAsnIle
NM_003140.2:c.305_306insCAATAT	NP_003131.1:p.Thr102_Glu103insAsnIle
NM_003140.3:c.305_306insCAATAT MANE Select	NP_003131.1:p.Thr102_Glu103insAsnIle