Canonical Allele Identifier: CA344235954

Gene: GPR37L1

Linked Data

• gnomAD v4: 1-202128335-G-C
• MyVariant Identifiers: chr1:g.202097463G>C (hg19) ; chr1:g.202128335G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128335G>C , CM000663.2:g.202128335G>C	GRCh38
NC_000001.10:g.202097463G>C , CM000663.1:g.202097463G>C	GRCh37
NC_000001.9:g.200364086G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.806G>C
ENST00000682545.1:c.*231G>C	ENSP00000508402.1:n.*231G>C
ENST00000682887.1:c.1626G>C	ENSP00000506946.1:n.1626G>C
ENST00000683302.1:c.1156G>C	ENSP00000507885.1:p.Gly386Arg
ENST00000683557.1:c.*57G>C	ENSP00000508029.1:n.*57G>C
ENST00000367282.6:c.1225G>C MANE Select	ENSP00000356251.4:p.Gly409Arg
ENST00000367282.5:c.1225G>C	ENSP00000356251.4:p.Gly409Arg
NM_004767.3:c.1225G>C	NP_004758.3:p.Gly409Arg
XM_011510158.1:c.664G>C	XP_011508460.1:p.Gly222Arg
NM_004767.4:c.1225G>C	NP_004758.3:p.Gly409Arg
XM_011510158.2:c.664G>C	XP_011508460.1:p.Gly222Arg
NM_004767.5:c.1225G>C MANE Select	NP_004758.3:p.Gly409Arg