Canonical Allele Identifier: CA1330213

Gene: GPR37L1

Linked Data

• dbSNP Id: rs138003036
• ExAC: 1:202097508 G / T
• gnomAD v2: 1-202097508-G-T
• MyVariant Identifiers: chr1:g.202097508G>T (hg19) ; chr1:g.202128380G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128380G>T , CM000663.2:g.202128380G>T	GRCh38
NC_000001.10:g.202097508G>T , CM000663.1:g.202097508G>T	GRCh37
NC_000001.9:g.200364131G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.851G>T
ENST00000682545.1:c.*276G>T	ENSP00000508402.1:n.*276G>T
ENST00000682887.1:c.1671G>T	ENSP00000506946.1:n.1671G>T
ENST00000683302.1:c.1201G>T	ENSP00000507885.1:p.Gly401Cys
ENST00000683557.1:c.*102G>T	ENSP00000508029.1:n.*102G>T
ENST00000367282.6:c.1270G>T MANE Select	ENSP00000356251.4:p.Gly424Cys
ENST00000367282.5:c.1270G>T	ENSP00000356251.4:p.Gly424Cys
NM_004767.3:c.1270G>T	NP_004758.3:p.Gly424Cys
XM_011510158.1:c.709G>T	XP_011508460.1:p.Gly237Cys
NM_004767.4:c.1270G>T	NP_004758.3:p.Gly424Cys
XM_011510158.2:c.709G>T	XP_011508460.1:p.Gly237Cys
NM_004767.5:c.1270G>T MANE Select	NP_004758.3:p.Gly424Cys