Canonical Allele Identifier: CA344235801

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1571713620
• MyVariant Identifiers: chr1:g.202097389A>C (hg19) ; chr1:g.202128261A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128261A>C , CM000663.2:g.202128261A>C	GRCh38
NC_000001.10:g.202097389A>C , CM000663.1:g.202097389A>C	GRCh37
NC_000001.9:g.200364012A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.732A>C
ENST00000682545.1:c.*157A>C	ENSP00000508402.1:n.*157A>C
ENST00000682887.1:c.1552A>C	ENSP00000506946.1:n.1552A>C
ENST00000683302.1:c.1082A>C	ENSP00000507885.1:p.Tyr361Ser
ENST00000683557.1:c.742A>C	ENSP00000508029.1:p.Thr248Pro
ENST00000367282.6:c.1151A>C MANE Select	ENSP00000356251.4:p.Tyr384Ser
ENST00000367282.5:c.1151A>C	ENSP00000356251.4:p.Tyr384Ser
NM_004767.3:c.1151A>C	NP_004758.3:p.Tyr384Ser
XM_011510158.1:c.590A>C	XP_011508460.1:p.Tyr197Ser
NM_004767.4:c.1151A>C	NP_004758.3:p.Tyr384Ser
XM_011510158.2:c.590A>C	XP_011508460.1:p.Tyr197Ser
NM_004767.5:c.1151A>C MANE Select	NP_004758.3:p.Tyr384Ser