Canonical Allele Identifier: CA414941935

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655602C>G (hg19) ; chrY:g.2787561C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787561C>G , CM000686.2:g.2787561C>G	GRCh38
NC_000024.9:g.2655602C>G , CM000686.1:g.2655602C>G	GRCh37
NC_000024.8:g.2715602C>G	NCBI36
NG_011751.1:g.5191G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12822C>G
ENST00000679825.1:n.673C>G
ENST00000680285.1:n.320-2188C>G
ENST00000680845.1:n.247C>G
ENST00000681787.1:n.106+12822C>G
ENST00000681940.1:n.106+12822C>G
ENST00000383070.2:c.43G>C MANE Select	ENSP00000372547.1:p.Asp15His
ENST00000383070.1:c.43G>C	ENSP00000372547.1:p.Asp15His
NM_003140.2:c.43G>C	NP_003131.1:p.Asp15His
NM_003140.3:c.43G>C MANE Select	NP_003131.1:p.Asp15His