Canonical Allele Identifier: CA344236077

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1558302634
• gnomAD v2: 1-202097524-A-T
• gnomAD v3: 1-202128396-A-T
• gnomAD v4: 1-202128396-A-T
• MyVariant Identifiers: chr1:g.202097524A>T (hg19) ; chr1:g.202097524_202097527delinsTCTG (hg19) ; chr1:g.202097524_202097530delinsTCTGCTG (hg19) ; chr1:g.202128396A>T (hg38) ; chr1:g.202128396_202128399delinsTCTG (hg38) ; chr1:g.202128396_202128402delinsTCTGCTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128396A>T , CM000663.2:g.202128396A>T	GRCh38
NC_000001.10:g.202097524A>T , CM000663.1:g.202097524A>T	GRCh37
NC_000001.9:g.200364147A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.867A>T
ENST00000682545.1:c.*292A>T	ENSP00000508402.1:n.*292A>T
ENST00000682887.1:c.1687A>T	ENSP00000506946.1:n.1687A>T
ENST00000683302.1:c.1217A>T	ENSP00000507885.1:p.Asp406Val
ENST00000683557.1:c.*118A>T	ENSP00000508029.1:n.*118A>T
ENST00000367282.6:c.1286A>T MANE Select	ENSP00000356251.4:p.Asp429Val
ENST00000367282.5:c.1286A>T	ENSP00000356251.4:p.Asp429Val
NM_004767.3:c.1286A>T	NP_004758.3:p.Asp429Val
XM_011510158.1:c.725A>T	XP_011508460.1:p.Asp242Val
NM_004767.4:c.1286A>T	NP_004758.3:p.Asp429Val
XM_011510158.2:c.725A>T	XP_011508460.1:p.Asp242Val
NM_004767.5:c.1286A>T MANE Select	NP_004758.3:p.Asp429Val