Canonical Allele Identifier: CA422796332

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1654732224
• MyVariant Identifiers: chr1:g.202097429G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128301G>C , CM000663.2:g.202128301G>C	GRCh38
NC_000001.10:g.202097429G>C , CM000663.1:g.202097429G>C	GRCh37
NC_000001.9:g.200364052G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.772G>C
ENST00000682545.1:c.*197G>C	ENSP00000508402.1:n.*197G>C
ENST00000682887.1:c.1592G>C	ENSP00000506946.1:n.1592G>C
ENST00000683302.1:c.1122G>C	ENSP00000507885.1:p.Leu374=
ENST00000683557.1:c.*23G>C	ENSP00000508029.1:n.*23G>C
ENST00000367282.6:c.1191G>C MANE Select	ENSP00000356251.4:p.Leu397=
ENST00000367282.5:c.1191G>C	ENSP00000356251.4:p.Leu397=
NM_004767.3:c.1191G>C	NP_004758.3:p.Leu397=
XM_011510158.1:c.630G>C	XP_011508460.1:p.Leu210=
NM_004767.4:c.1191G>C	NP_004758.3:p.Leu397=
XM_011510158.2:c.630G>C	XP_011508460.1:p.Leu210=
NM_004767.5:c.1191G>C MANE Select	NP_004758.3:p.Leu397=