Canonical Allele Identifier: CA1330230

Gene: GPR37L1

Linked Data

• dbSNP Id: rs778049527
• ExAC: 1:202097576 T / C
• gnomAD v2: 1-202097576-T-C
• gnomAD v3: 1-202128448-T-C
• gnomAD v4: 1-202128448-T-C
• MyVariant Identifiers: chr1:g.202097576T>C (hg19) ; chr1:g.202128448T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128448T>C , CM000663.2:g.202128448T>C	GRCh38
NC_000001.10:g.202097576T>C , CM000663.1:g.202097576T>C	GRCh37
NC_000001.9:g.200364199T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.919T>C
ENST00000682545.1:c.*344T>C	ENSP00000508402.1:n.*344T>C
ENST00000682887.1:c.1739T>C	ENSP00000506946.1:n.1739T>C
ENST00000683302.1:c.1269T>C	ENSP00000507885.1:p.Ser423=
ENST00000683557.1:c.*170T>C	ENSP00000508029.1:n.*170T>C
ENST00000367282.6:c.1338T>C MANE Select	ENSP00000356251.4:p.Ser446=
ENST00000367282.5:c.1338T>C	ENSP00000356251.4:p.Ser446=
NM_004767.3:c.1338T>C	NP_004758.3:p.Ser446=
XM_011510158.1:c.777T>C	XP_011508460.1:p.Ser259=
NM_004767.4:c.1338T>C	NP_004758.3:p.Ser446=
XM_011510158.2:c.777T>C	XP_011508460.1:p.Ser259=
NM_004767.5:c.1338T>C MANE Select	NP_004758.3:p.Ser446=