Canonical Allele Identifier: CA344235781

Gene: GPR37L1

Linked Data

• gnomAD v4: 1-202128250-C-G
• MyVariant Identifiers: chr1:g.202097378C>G (hg19) ; chr1:g.202128250C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128250C>G , CM000663.2:g.202128250C>G	GRCh38
NC_000001.10:g.202097378C>G , CM000663.1:g.202097378C>G	GRCh37
NC_000001.9:g.200364001C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.721C>G
ENST00000682545.1:c.*146C>G	ENSP00000508402.1:n.*146C>G
ENST00000682887.1:c.1541C>G	ENSP00000506946.1:n.1541C>G
ENST00000683302.1:c.1071C>G	ENSP00000507885.1:p.Ile357Met
ENST00000683557.1:c.731C>G	ENSP00000508029.1:p.Ser244Trp
ENST00000367282.6:c.1140C>G MANE Select	ENSP00000356251.4:p.Ile380Met
ENST00000367282.5:c.1140C>G	ENSP00000356251.4:p.Ile380Met
NM_004767.3:c.1140C>G	NP_004758.3:p.Ile380Met
XM_011510158.1:c.579C>G	XP_011508460.1:p.Ile193Met
NM_004767.4:c.1140C>G	NP_004758.3:p.Ile380Met
XM_011510158.2:c.579C>G	XP_011508460.1:p.Ile193Met
NM_004767.5:c.1140C>G MANE Select	NP_004758.3:p.Ile380Met