Canonical Allele Identifier: CA414941358

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655352C>T (hg19) ; chrY:g.2787311C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787311C>T , CM000686.2:g.2787311C>T	GRCh38
NC_000024.9:g.2655352C>T , CM000686.1:g.2655352C>T	GRCh37
NC_000024.8:g.2715352C>T	NCBI36
NG_011751.1:g.5441G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+12572C>T
ENST00000679825.1:n.423C>T
ENST00000680285.1:n.320-2438C>T
ENST00000680845.1:n.166-169C>T
ENST00000681787.1:n.106+12572C>T
ENST00000681940.1:n.106+12572C>T
ENST00000383070.2:c.293G>A MANE Select	ENSP00000372547.1:p.Trp98Ter
ENST00000383070.1:c.293G>A	ENSP00000372547.1:p.Trp98Ter
NM_003140.2:c.293G>A	NP_003131.1:p.Trp98Ter
NM_003140.3:c.293G>A MANE Select	NP_003131.1:p.Trp98Ter