Canonical Allele Identifier: CA344236074

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1465148456
• MyVariant Identifiers: chr1:g.202097523G>T (hg19) ; chr1:g.202128395G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128395G>T , CM000663.2:g.202128395G>T	GRCh38
NC_000001.10:g.202097523G>T , CM000663.1:g.202097523G>T	GRCh37
NC_000001.9:g.200364146G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.866G>T
ENST00000682545.1:c.*291G>T	ENSP00000508402.1:n.*291G>T
ENST00000682887.1:c.1686G>T	ENSP00000506946.1:n.1686G>T
ENST00000683302.1:c.1216G>T	ENSP00000507885.1:p.Asp406Tyr
ENST00000683557.1:c.*117G>T	ENSP00000508029.1:n.*117G>T
ENST00000367282.6:c.1285G>T MANE Select	ENSP00000356251.4:p.Asp429Tyr
ENST00000367282.5:c.1285G>T	ENSP00000356251.4:p.Asp429Tyr
NM_004767.3:c.1285G>T	NP_004758.3:p.Asp429Tyr
XM_011510158.1:c.724G>T	XP_011508460.1:p.Asp242Tyr
NM_004767.4:c.1285G>T	NP_004758.3:p.Asp429Tyr
XM_011510158.2:c.724G>T	XP_011508460.1:p.Asp242Tyr
NM_004767.5:c.1285G>T MANE Select	NP_004758.3:p.Asp429Tyr