Canonical Allele Identifier: CA414941084

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655238T>A (hg19) ; chrY:g.2787197T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787197T>A , CM000686.2:g.2787197T>A	GRCh38
NC_000024.9:g.2655238T>A , CM000686.1:g.2655238T>A	GRCh37
NC_000024.8:g.2715238T>A	NCBI36
NG_011751.1:g.5555A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+12458T>A
ENST00000679825.1:n.309T>A
ENST00000680285.1:n.320-2552T>A
ENST00000680845.1:n.165+144T>A
ENST00000681787.1:n.106+12458T>A
ENST00000681940.1:n.106+12458T>A
ENST00000383070.2:c.407A>T MANE Select	ENSP00000372547.1:p.Lys136Met
ENST00000383070.1:c.407A>T	ENSP00000372547.1:p.Lys136Met
NM_003140.2:c.407A>T	NP_003131.1:p.Lys136Met
NM_003140.3:c.407A>T MANE Select	NP_003131.1:p.Lys136Met