Canonical Allele Identifier: CA1330157

Gene: GPR37L1

Linked Data

• ClinVar Variation Id: 522590
• ClinVar RCV Id: RCV000625728
• dbSNP Id: rs372386575
• ExAC: 1:202097285 G / T
• gnomAD v2: 1-202097285-G-T
• gnomAD v3: 1-202128157-G-T
• gnomAD v4: 1-202128157-G-T
• MyVariant Identifiers: chr1:g.202097285G>T (hg19) ; chr1:g.202128157G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128157G>T , CM000663.2:g.202128157G>T	GRCh38
NC_000001.10:g.202097285G>T , CM000663.1:g.202097285G>T	GRCh37
NC_000001.9:g.200363908G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000682422.1:n.705-77G>T
ENST00000682545.1:c.*53G>T	ENSP00000508402.1:n.*53G>T
ENST00000682887.1:c.1448G>T	ENSP00000506946.1:n.1448G>T
ENST00000683302.1:c.978G>T	ENSP00000507885.1:p.Lys326Asn
ENST00000683457.1:n.569G>T
ENST00000683557.1:c.715-77G>T	ENSP00000508029.1:n.715-77G>T
ENST00000367282.6:c.1047G>T MANE Select	ENSP00000356251.4:p.Lys349Asn
ENST00000367282.5:c.1047G>T	ENSP00000356251.4:p.Lys349Asn
NM_004767.3:c.1047G>T	NP_004758.3:p.Lys349Asn
XM_011510158.1:c.486G>T	XP_011508460.1:p.Lys162Asn
NM_004767.4:c.1047G>T	NP_004758.3:p.Lys349Asn
XM_011510158.2:c.486G>T	XP_011508460.1:p.Lys162Asn
NM_004767.5:c.1047G>T MANE Select	NP_004758.3:p.Lys349Asn