Canonical Allele Identifier: CA344236174

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1571713827
• MyVariant Identifiers: chr1:g.202097562G>T (hg19) ; chr1:g.202128434G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128434G>T , CM000663.2:g.202128434G>T	GRCh38
NC_000001.10:g.202097562G>T , CM000663.1:g.202097562G>T	GRCh37
NC_000001.9:g.200364185G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.905G>T
ENST00000682545.1:c.*330G>T	ENSP00000508402.1:n.*330G>T
ENST00000682887.1:c.1725G>T	ENSP00000506946.1:n.1725G>T
ENST00000683302.1:c.1255G>T	ENSP00000507885.1:p.Ala419Ser
ENST00000683557.1:c.*156G>T	ENSP00000508029.1:n.*156G>T
ENST00000367282.6:c.1324G>T MANE Select	ENSP00000356251.4:p.Ala442Ser
ENST00000367282.5:c.1324G>T	ENSP00000356251.4:p.Ala442Ser
NM_004767.3:c.1324G>T	NP_004758.3:p.Ala442Ser
XM_011510158.1:c.763G>T	XP_011508460.1:p.Ala255Ser
NM_004767.4:c.1324G>T	NP_004758.3:p.Ala442Ser
XM_011510158.2:c.763G>T	XP_011508460.1:p.Ala255Ser
NM_004767.5:c.1324G>T MANE Select	NP_004758.3:p.Ala442Ser