Canonical Allele Identifier: CA1330214

Gene: GPR37L1

Linked Data

• dbSNP Id: rs762972110
• ExAC: 1:202097511 C / G
• gnomAD v2: 1-202097511-C-G
• gnomAD v4: 1-202128383-C-G
• MyVariant Identifiers: chr1:g.202097511C>G (hg19) ; chr1:g.202128383C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128383C>G , CM000663.2:g.202128383C>G	GRCh38
NC_000001.10:g.202097511C>G , CM000663.1:g.202097511C>G	GRCh37
NC_000001.9:g.200364134C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.854C>G
ENST00000682545.1:c.*279C>G	ENSP00000508402.1:n.*279C>G
ENST00000682887.1:c.1674C>G	ENSP00000506946.1:n.1674C>G
ENST00000683302.1:c.1204C>G	ENSP00000507885.1:p.Gln402Glu
ENST00000683557.1:c.*105C>G	ENSP00000508029.1:n.*105C>G
ENST00000367282.6:c.1273C>G MANE Select	ENSP00000356251.4:p.Gln425Glu
ENST00000367282.5:c.1273C>G	ENSP00000356251.4:p.Gln425Glu
NM_004767.3:c.1273C>G	NP_004758.3:p.Gln425Glu
XM_011510158.1:c.712C>G	XP_011508460.1:p.Gln238Glu
NM_004767.4:c.1273C>G	NP_004758.3:p.Gln425Glu
XM_011510158.2:c.712C>G	XP_011508460.1:p.Gln238Glu
NM_004767.5:c.1273C>G MANE Select	NP_004758.3:p.Gln425Glu