Canonical Allele Identifier: CA344235963

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1654734947
• MyVariant Identifiers: chr1:g.202097467C>T (hg19) ; chr1:g.202128339C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128339C>T , CM000663.2:g.202128339C>T	GRCh38
NC_000001.10:g.202097467C>T , CM000663.1:g.202097467C>T	GRCh37
NC_000001.9:g.200364090C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.810C>T
ENST00000682545.1:c.*235C>T	ENSP00000508402.1:n.*235C>T
ENST00000682887.1:c.1630C>T	ENSP00000506946.1:n.1630C>T
ENST00000683302.1:c.1160C>T	ENSP00000507885.1:p.Ala387Val
ENST00000683557.1:c.*61C>T	ENSP00000508029.1:n.*61C>T
ENST00000367282.6:c.1229C>T MANE Select	ENSP00000356251.4:p.Ala410Val
ENST00000367282.5:c.1229C>T	ENSP00000356251.4:p.Ala410Val
NM_004767.3:c.1229C>T	NP_004758.3:p.Ala410Val
XM_011510158.1:c.668C>T	XP_011508460.1:p.Ala223Val
NM_004767.4:c.1229C>T	NP_004758.3:p.Ala410Val
XM_011510158.2:c.668C>T	XP_011508460.1:p.Ala223Val
NM_004767.5:c.1229C>T MANE Select	NP_004758.3:p.Ala410Val