Canonical Allele Identifier: CA1330170

Gene: GPR37L1

Linked Data

• dbSNP Id: rs776045297
• ExAC: 1:202097323 T / C
• gnomAD v2: 1-202097323-T-C
• gnomAD v4: 1-202128195-T-C
• MyVariant Identifiers: chr1:g.202097323T>C (hg19) ; chr1:g.202128195T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128195T>C , CM000663.2:g.202128195T>C	GRCh38
NC_000001.10:g.202097323T>C , CM000663.1:g.202097323T>C	GRCh37
NC_000001.9:g.200363946T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.705-39T>C
ENST00000682545.1:c.*91T>C	ENSP00000508402.1:n.*91T>C
ENST00000682887.1:c.1486T>C	ENSP00000506946.1:n.1486T>C
ENST00000683302.1:c.1016T>C	ENSP00000507885.1:p.Val339Ala
ENST00000683557.1:c.715-39T>C	ENSP00000508029.1:n.715-39T>C
ENST00000367282.6:c.1085T>C MANE Select	ENSP00000356251.4:p.Val362Ala
ENST00000367282.5:c.1085T>C	ENSP00000356251.4:p.Val362Ala
NM_004767.3:c.1085T>C	NP_004758.3:p.Val362Ala
XM_011510158.1:c.524T>C	XP_011508460.1:p.Val175Ala
NM_004767.4:c.1085T>C	NP_004758.3:p.Val362Ala
XM_011510158.2:c.524T>C	XP_011508460.1:p.Val175Ala
NM_004767.5:c.1085T>C MANE Select	NP_004758.3:p.Val362Ala