Canonical Allele Identifier: CA414941948

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655607T>C (hg19) ; chrY:g.2787566T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787566T>C , CM000686.2:g.2787566T>C	GRCh38
NC_000024.9:g.2655607T>C , CM000686.1:g.2655607T>C	GRCh37
NC_000024.8:g.2715607T>C	NCBI36
NG_011751.1:g.5186A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+12827T>C
ENST00000679825.1:n.678T>C
ENST00000680285.1:n.320-2183T>C
ENST00000680845.1:n.252T>C
ENST00000681787.1:n.106+12827T>C
ENST00000681940.1:n.106+12827T>C
ENST00000383070.2:c.38A>G MANE Select	ENSP00000372547.1:p.Asn13Ser
ENST00000383070.1:c.38A>G	ENSP00000372547.1:p.Asn13Ser
NM_003140.2:c.38A>G	NP_003131.1:p.Asn13Ser
NM_003140.3:c.38A>G MANE Select	NP_003131.1:p.Asn13Ser