Canonical Allele Identifier: CA2469659933
Gene: SRY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786968A= , CM000686.2:g.2786968A= GRCh38
NC_000024.9:g.2655009A= , CM000686.1:g.2655009A= GRCh37
NC_000024.8:g.2715009A= NCBI36
NG_011751.1:g.5784T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12229A=
ENST00000679825.1:n.107-27A=
ENST00000680285.1:n.320-2781A=
ENST00000680845.1:n.107-27A=
ENST00000681787.1:n.106+12229A=
ENST00000681940.1:n.106+12229A=
ENST00000383070.2:c.*21T= MANE Select ENSP00000372547.1:n.*21T=
ENST00000383070.1:c.*21T= ENSP00000372547.1:n.*21T=
NM_003140.2:c.*21T= NP_003131.1:n.*21T=
NM_003140.3:c.*21T= MANE Select NP_003131.1:n.*21T=