Canonical Allele Identifier: CA519429406

Gene: SRY

Linked Data

• MyVariant Identifiers: chrY:g.2655033C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2786992C>A , CM000686.2:g.2786992C>A	GRCh38
NC_000024.9:g.2655033C>A , CM000686.1:g.2655033C>A	GRCh37
NC_000024.8:g.2715033C>A	NCBI36
NG_011751.1:g.5760G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+12253C>A
ENST00000679825.1:n.107-3C>A
ENST00000680285.1:n.320-2757C>A
ENST00000680845.1:n.107-3C>A
ENST00000681787.1:n.106+12253C>A
ENST00000681940.1:n.106+12253C>A
ENST00000383070.2:c.612G>T MANE Select	ENSP00000372547.1:p.Leu204=
ENST00000383070.1:c.612G>T	ENSP00000372547.1:p.Leu204=
NM_003140.2:c.612G>T	NP_003131.1:p.Leu204=
NM_003140.3:c.612G>T MANE Select	NP_003131.1:p.Leu204=