Canonical Allele Identifier: CA1330199

Gene: GPR37L1

Linked Data

• dbSNP Id: rs375520473
• ExAC: 1:202097462 G / A
• gnomAD v2: 1-202097462-G-A
• MyVariant Identifiers: chr1:g.202097462G>A (hg19) ; chr1:g.202128334G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128334G>A , CM000663.2:g.202128334G>A	GRCh38
NC_000001.10:g.202097462G>A , CM000663.1:g.202097462G>A	GRCh37
NC_000001.9:g.200364085G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.805G>A
ENST00000682545.1:c.*230G>A	ENSP00000508402.1:n.*230G>A
ENST00000682887.1:c.1625G>A	ENSP00000506946.1:n.1625G>A
ENST00000683302.1:c.1155G>A	ENSP00000507885.1:p.Lys385=
ENST00000683557.1:c.*56G>A	ENSP00000508029.1:n.*56G>A
ENST00000367282.6:c.1224G>A MANE Select	ENSP00000356251.4:p.Lys408=
ENST00000367282.5:c.1224G>A	ENSP00000356251.4:p.Lys408=
NM_004767.3:c.1224G>A	NP_004758.3:p.Lys408=
XM_011510158.1:c.663G>A	XP_011508460.1:p.Lys221=
NM_004767.4:c.1224G>A	NP_004758.3:p.Lys408=
XM_011510158.2:c.663G>A	XP_011508460.1:p.Lys221=
NM_004767.5:c.1224G>A MANE Select	NP_004758.3:p.Lys408=