Canonical Allele Identifier: CA422553954

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1558302678
• gnomAD v4: 1-202128434-GC-G
• MyVariant Identifiers: chr1:g.202097563del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128435del , CM000663.2:g.202128435del	GRCh38
NC_000001.10:g.202097563del , CM000663.1:g.202097563del	GRCh37
NC_000001.9:g.200364186del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.906del
ENST00000682545.1:c.*331del	ENSP00000508402.1:n.*331del
ENST00000682887.1:c.1726del	ENSP00000506946.1:n.1726del
ENST00000683302.1:c.1256del	ENSP00000507885.1:p.Ala419ValfsTer?
ENST00000683557.1:c.*157del	ENSP00000508029.1:n.*157del
ENST00000367282.6:c.1325del MANE Select	ENSP00000356251.4:p.Ala442ValfsTer?
ENST00000367282.5:c.1325del	ENSP00000356251.4:p.Ala442ValfsTer?
NM_004767.3:c.1325del	NP_004758.3:p.Ala442ValfsTer?
XM_011510158.1:c.764del	XP_011508460.1:p.Ala255ValfsTer?
NM_004767.4:c.1325del	NP_004758.3:p.Ala442ValfsTer?
XM_011510158.2:c.764del	XP_011508460.1:p.Ala255ValfsTer?
NM_004767.5:c.1325del MANE Select	NP_004758.3:p.Ala442ValfsTer?