Canonical Allele Identifier: CA415270090

Gene: GPR50

Linked Data

• MyVariant Identifiers: chrX:g.150349835A>G (hg19) ; chrX:g.151181363A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181363A>G , CM000685.2:g.151181363A>G	GRCh38
NC_000023.10:g.150349835A>G , CM000685.1:g.150349835A>G	GRCh37
NC_000023.9:g.150100493A>G	NCBI36
NG_016405.1:g.9780A>G
NG_016405.2:g.9780A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218316.4:c.1780A>G MANE Select	ENSP00000218316.3:p.Thr594Ala
ENST00000218316.3:c.1780A>G	ENSP00000218316.3:p.Thr594Ala
ENST00000617907.1:c.1774A>G	ENSP00000484496.1:p.Thr592Ala
NM_004224.3:c.1780A>G MANE Select	NP_004215.2:p.Thr594Ala
XM_011531216.1:c.1039A>G	XP_011529518.1:p.Thr347Ala
XM_011531216.2:c.1039A>G	XP_011529518.1:p.Thr347Ala