Canonical Allele Identifier: CA2469660013
Gene: SRY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787648T= , CM000686.2:g.2787648T= GRCh38
NC_000024.9:g.2655689T= , CM000686.1:g.2655689T= GRCh37
NC_000024.8:g.2715689T= NCBI36
NG_011751.1:g.5104A=

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12909T=
ENST00000680285.1:n.320-2101T=
ENST00000681787.1:n.106+12909T=
ENST00000681940.1:n.106+12909T=
ENST00000383070.2:c.-45A= MANE Select ENSP00000372547.1:n.-45A=
ENST00000383070.1:c.-45A= ENSP00000372547.1:n.-45A=
NM_003140.2:c.-45A= NP_003131.1:n.-45A=
NM_003140.3:c.-45A= MANE Select NP_003131.1:n.-45A=