Canonical Allele Identifier: CA519131625

Gene: GPR50

Linked Data

• MyVariant Identifiers: chrX:g.150349771C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181299C>T , CM000685.2:g.151181299C>T	GRCh38
NC_000023.10:g.150349771C>T , CM000685.1:g.150349771C>T	GRCh37
NC_000023.9:g.150100429C>T	NCBI36
NG_016405.1:g.9716C>T
NG_016405.2:g.9716C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218316.4:c.1716C>T MANE Select	ENSP00000218316.3:p.Thr572=
ENST00000218316.3:c.1716C>T	ENSP00000218316.3:p.Thr572=
ENST00000617907.1:c.1710C>T	ENSP00000484496.1:p.Thr570=
NM_004224.3:c.1716C>T MANE Select	NP_004215.2:p.Thr572=
XM_011531216.1:c.975C>T	XP_011529518.1:p.Thr325=
XM_011531216.2:c.975C>T	XP_011529518.1:p.Thr325=