Canonical Allele Identifier: CA2649858832

Gene: GPR37L1

Linked Data

• gnomAD v4: 1-202128381-GC-G

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.854del
ENST00000682545.1:c.*279del	ENSP00000508402.1:n.*279del
ENST00000682887.1:c.1674del	ENSP00000506946.1:n.1674del
ENST00000683302.1:c.1204del	ENSP00000507885.1:p.Gln402ArgfsTer?
ENST00000683557.1:c.*105del	ENSP00000508029.1:n.*105del
ENST00000367282.6:c.1273del MANE Select	ENSP00000356251.4:p.Gln425ArgfsTer?
ENST00000367282.5:c.1273del	ENSP00000356251.4:p.Gln425ArgfsTer?
NM_004767.3:c.1273del	NP_004758.3:p.Gln425ArgfsTer?
XM_011510158.1:c.712del	XP_011508460.1:p.Gln238ArgfsTer?
NM_004767.4:c.1273del	NP_004758.3:p.Gln425ArgfsTer?
XM_011510158.2:c.712del	XP_011508460.1:p.Gln238ArgfsTer?
NM_004767.5:c.1273del MANE Select	NP_004758.3:p.Gln425ArgfsTer?