Canonical Allele Identifier: CA415269970

Gene: GPR50

Linked Data

• MyVariant Identifiers: chrX:g.150349778G>T (hg19) ; chrX:g.151181306G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181306G>T , CM000685.2:g.151181306G>T	GRCh38
NC_000023.10:g.150349778G>T , CM000685.1:g.150349778G>T	GRCh37
NC_000023.9:g.150100436G>T	NCBI36
NG_016405.1:g.9723G>T
NG_016405.2:g.9723G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218316.4:c.1723G>T MANE Select	ENSP00000218316.3:p.Ala575Ser
ENST00000218316.3:c.1723G>T	ENSP00000218316.3:p.Ala575Ser
ENST00000617907.1:c.1717G>T	ENSP00000484496.1:p.Ala573Ser
NM_004224.3:c.1723G>T MANE Select	NP_004215.2:p.Ala575Ser
XM_011531216.1:c.982G>T	XP_011529518.1:p.Ala328Ser
XM_011531216.2:c.982G>T	XP_011529518.1:p.Ala328Ser