Canonical Allele Identifier: CA519724536

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655603G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787562G>A , CM000686.2:g.2787562G>A	GRCh38
NC_000024.9:g.2655603G>A , CM000686.1:g.2655603G>A	GRCh37
NC_000024.8:g.2715603G>A	NCBI36
NG_011751.1:g.5190C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+12823G>A
ENST00000679825.1:n.674G>A
ENST00000680285.1:n.320-2187G>A
ENST00000680845.1:n.248G>A
ENST00000681787.1:n.106+12823G>A
ENST00000681940.1:n.106+12823G>A
ENST00000383070.2:c.42C>T MANE Select	ENSP00000372547.1:p.Ser14=
ENST00000383070.1:c.42C>T	ENSP00000372547.1:p.Ser14=
NM_003140.2:c.42C>T	NP_003131.1:p.Ser14=
NM_003140.3:c.42C>T MANE Select	NP_003131.1:p.Ser14=