Canonical Allele Identifier: CA2469659927
Gene: SRY HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786919G= , CM000686.2:g.2786919G= GRCh38
NC_000024.9:g.2654960G= , CM000686.1:g.2654960G= GRCh37
NC_000024.8:g.2714960G= NCBI36
NG_011751.1:g.5833C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12180G=
ENST00000679825.1:n.107-76G=
ENST00000680285.1:n.320-2830G=
ENST00000680845.1:n.107-76G=
ENST00000681787.1:n.106+12180G=
ENST00000681940.1:n.106+12180G=
ENST00000383070.2:c.*70C= MANE Select ENSP00000372547.1:n.*70C=
ENST00000383070.1:c.*70C= ENSP00000372547.1:n.*70C=
NM_003140.2:c.*70C= NP_003131.1:n.*70C=
NM_003140.3:c.*70C= MANE Select NP_003131.1:n.*70C=
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