Canonical Allele Identifier: CA2766266499

Gene: SRY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787606T>A , CM000686.2:g.2787606T>A	GRCh38
NC_000024.9:g.2655647T>A , CM000686.1:g.2655647T>A	GRCh37
NC_000024.8:g.2715647T>A	NCBI36
NG_011751.1:g.5146A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12867T>A
ENST00000680285.1:n.320-2143T>A
ENST00000680845.1:n.292T>A
ENST00000681787.1:n.106+12867T>A
ENST00000681940.1:n.106+12867T>A
ENST00000383070.2:c.-3A>T MANE Select	ENSP00000372547.1:n.-3A>T
ENST00000383070.1:c.-3A>T	ENSP00000372547.1:n.-3A>T
NM_003140.2:c.-3A>T	NP_003131.1:n.-3A>T
NM_003140.3:c.-3A>T MANE Select	NP_003131.1:n.-3A>T