Canonical Allele Identifier: CA1330198

Gene: GPR37L1

Linked Data

• dbSNP Id: rs763981644
• ExAC: 1:202097459 C / G
• gnomAD v2: 1-202097459-C-G
• gnomAD v4: 1-202128331-C-G
• MyVariant Identifiers: chr1:g.202097459C>G (hg19) ; chr1:g.202128331C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128331C>G , CM000663.2:g.202128331C>G	GRCh38
NC_000001.10:g.202097459C>G , CM000663.1:g.202097459C>G	GRCh37
NC_000001.9:g.200364082C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.802C>G
ENST00000682545.1:c.*227C>G	ENSP00000508402.1:n.*227C>G
ENST00000682887.1:c.1622C>G	ENSP00000506946.1:n.1622C>G
ENST00000683302.1:c.1152C>G	ENSP00000507885.1:p.Phe384Leu
ENST00000683557.1:c.*53C>G	ENSP00000508029.1:n.*53C>G
ENST00000367282.6:c.1221C>G MANE Select	ENSP00000356251.4:p.Phe407Leu
ENST00000367282.5:c.1221C>G	ENSP00000356251.4:p.Phe407Leu
NM_004767.3:c.1221C>G	NP_004758.3:p.Phe407Leu
XM_011510158.1:c.660C>G	XP_011508460.1:p.Phe220Leu
NM_004767.4:c.1221C>G	NP_004758.3:p.Phe407Leu
XM_011510158.2:c.660C>G	XP_011508460.1:p.Phe220Leu
NM_004767.5:c.1221C>G MANE Select	NP_004758.3:p.Phe407Leu