Canonical Allele Identifier: CA344236180

Gene: GPR37L1

Linked Data

• ClinVar Variation Id: 2387148
• ClinVar RCV Id: RCV004218147
• dbSNP Id: rs1246374793
• gnomAD v2: 1-202097565-T-C
• gnomAD v3: 1-202128437-T-C
• gnomAD v4: 1-202128437-T-C
• MyVariant Identifiers: chr1:g.202097565T>C (hg19) ; chr1:g.202128437T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128437T>C , CM000663.2:g.202128437T>C	GRCh38
NC_000001.10:g.202097565T>C , CM000663.1:g.202097565T>C	GRCh37
NC_000001.9:g.200364188T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.908T>C
ENST00000682545.1:c.*333T>C	ENSP00000508402.1:n.*333T>C
ENST00000682887.1:c.1728T>C	ENSP00000506946.1:n.1728T>C
ENST00000683302.1:c.1258T>C	ENSP00000507885.1:p.Ser420Pro
ENST00000683557.1:c.*159T>C	ENSP00000508029.1:n.*159T>C
ENST00000367282.6:c.1327T>C MANE Select	ENSP00000356251.4:p.Ser443Pro
ENST00000367282.5:c.1327T>C	ENSP00000356251.4:p.Ser443Pro
NM_004767.3:c.1327T>C	NP_004758.3:p.Ser443Pro
XM_011510158.1:c.766T>C	XP_011508460.1:p.Ser256Pro
NM_004767.4:c.1327T>C	NP_004758.3:p.Ser443Pro
XM_011510158.2:c.766T>C	XP_011508460.1:p.Ser256Pro
NM_004767.5:c.1327T>C MANE Select	NP_004758.3:p.Ser443Pro