Canonical Allele Identifier: CA344236151

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097551A>C (hg19) ; chr1:g.202128423A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128423A>C , CM000663.2:g.202128423A>C	GRCh38
NC_000001.10:g.202097551A>C , CM000663.1:g.202097551A>C	GRCh37
NC_000001.9:g.200364174A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.894A>C
ENST00000682545.1:c.*319A>C	ENSP00000508402.1:n.*319A>C
ENST00000682887.1:c.1714A>C	ENSP00000506946.1:n.1714A>C
ENST00000683302.1:c.1244A>C	ENSP00000507885.1:p.Glu415Ala
ENST00000683557.1:c.*145A>C	ENSP00000508029.1:n.*145A>C
ENST00000367282.6:c.1313A>C MANE Select	ENSP00000356251.4:p.Glu438Ala
ENST00000367282.5:c.1313A>C	ENSP00000356251.4:p.Glu438Ala
NM_004767.3:c.1313A>C	NP_004758.3:p.Glu438Ala
XM_011510158.1:c.752A>C	XP_011508460.1:p.Glu251Ala
NM_004767.4:c.1313A>C	NP_004758.3:p.Glu438Ala
XM_011510158.2:c.752A>C	XP_011508460.1:p.Glu251Ala
NM_004767.5:c.1313A>C MANE Select	NP_004758.3:p.Glu438Ala