Canonical Allele Identifier: CA1330210

Gene: GPR37L1

Linked Data

• dbSNP Id: rs773413931
• ExAC: 1:202097503 C / T
• gnomAD v2: 1-202097503-C-T
• gnomAD v3: 1-202128375-C-T
• gnomAD v4: 1-202128375-C-T
• COSMIC: COSM1668373
• MyVariant Identifiers: chr1:g.202097503C>T (hg19) ; chr1:g.202128375C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128375C>T , CM000663.2:g.202128375C>T	GRCh38
NC_000001.10:g.202097503C>T , CM000663.1:g.202097503C>T	GRCh37
NC_000001.9:g.200364126C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.846C>T
ENST00000682545.1:c.*271C>T	ENSP00000508402.1:n.*271C>T
ENST00000682887.1:c.1666C>T	ENSP00000506946.1:n.1666C>T
ENST00000683302.1:c.1196C>T	ENSP00000507885.1:p.Pro399Leu
ENST00000683557.1:c.*97C>T	ENSP00000508029.1:n.*97C>T
ENST00000367282.6:c.1265C>T MANE Select	ENSP00000356251.4:p.Pro422Leu
ENST00000367282.5:c.1265C>T	ENSP00000356251.4:p.Pro422Leu
NM_004767.3:c.1265C>T	NP_004758.3:p.Pro422Leu
XM_011510158.1:c.704C>T	XP_011508460.1:p.Pro235Leu
NM_004767.4:c.1265C>T	NP_004758.3:p.Pro422Leu
XM_011510158.2:c.704C>T	XP_011508460.1:p.Pro235Leu
NM_004767.5:c.1265C>T MANE Select	NP_004758.3:p.Pro422Leu