Canonical Allele Identifier: CA2766266493

Gene: SRY

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2786944A>C , CM000686.2:g.2786944A>C	GRCh38
NC_000024.9:g.2654985A>C , CM000686.1:g.2654985A>C	GRCh37
NC_000024.8:g.2714985A>C	NCBI36
NG_011751.1:g.5808T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12205A>C
ENST00000679825.1:n.107-51A>C
ENST00000680285.1:n.320-2805A>C
ENST00000680845.1:n.107-51A>C
ENST00000681787.1:n.106+12205A>C
ENST00000681940.1:n.106+12205A>C
ENST00000383070.2:c.*45T>G MANE Select	ENSP00000372547.1:n.*45T>G
ENST00000383070.1:c.*45T>G	ENSP00000372547.1:n.*45T>G
NM_003140.2:c.*45T>G	NP_003131.1:n.*45T>G
NM_003140.3:c.*45T>G MANE Select	NP_003131.1:n.*45T>G