Canonical Allele Identifier: CA344236063

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097518T>C (hg19) ; chr1:g.202128390T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128390T>C , CM000663.2:g.202128390T>C	GRCh38
NC_000001.10:g.202097518T>C , CM000663.1:g.202097518T>C	GRCh37
NC_000001.9:g.200364141T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.861T>C
ENST00000682545.1:c.*286T>C	ENSP00000508402.1:n.*286T>C
ENST00000682887.1:c.1681T>C	ENSP00000506946.1:n.1681T>C
ENST00000683302.1:c.1211T>C	ENSP00000507885.1:p.Phe404Ser
ENST00000683557.1:c.*112T>C	ENSP00000508029.1:n.*112T>C
ENST00000367282.6:c.1280T>C MANE Select	ENSP00000356251.4:p.Phe427Ser
ENST00000367282.5:c.1280T>C	ENSP00000356251.4:p.Phe427Ser
NM_004767.3:c.1280T>C	NP_004758.3:p.Phe427Ser
XM_011510158.1:c.719T>C	XP_011508460.1:p.Phe240Ser
NM_004767.4:c.1280T>C	NP_004758.3:p.Phe427Ser
XM_011510158.2:c.719T>C	XP_011508460.1:p.Phe240Ser
NM_004767.5:c.1280T>C MANE Select	NP_004758.3:p.Phe427Ser