Canonical Allele Identifier: CA422553956

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097564T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128436T>C , CM000663.2:g.202128436T>C	GRCh38
NC_000001.10:g.202097564T>C , CM000663.1:g.202097564T>C	GRCh37
NC_000001.9:g.200364187T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.907T>C
ENST00000682545.1:c.*332T>C	ENSP00000508402.1:n.*332T>C
ENST00000682887.1:c.1727T>C	ENSP00000506946.1:n.1727T>C
ENST00000683302.1:c.1257T>C	ENSP00000507885.1:p.Ala419=
ENST00000683557.1:c.*158T>C	ENSP00000508029.1:n.*158T>C
ENST00000367282.6:c.1326T>C MANE Select	ENSP00000356251.4:p.Ala442=
ENST00000367282.5:c.1326T>C	ENSP00000356251.4:p.Ala442=
NM_004767.3:c.1326T>C	NP_004758.3:p.Ala442=
XM_011510158.1:c.765T>C	XP_011508460.1:p.Ala255=
NM_004767.4:c.1326T>C	NP_004758.3:p.Ala442=
XM_011510158.2:c.765T>C	XP_011508460.1:p.Ala255=
NM_004767.5:c.1326T>C MANE Select	NP_004758.3:p.Ala442=