Canonical Allele Identifier: CA344236137

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1294340594
• gnomAD v2: 1-202097547-G-T
• gnomAD v4: 1-202128419-G-T
• MyVariant Identifiers: chr1:g.202097547G>T (hg19) ; chr1:g.202128419G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128419G>T , CM000663.2:g.202128419G>T	GRCh38
NC_000001.10:g.202097547G>T , CM000663.1:g.202097547G>T	GRCh37
NC_000001.9:g.200364170G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.890G>T
ENST00000682545.1:c.*315G>T	ENSP00000508402.1:n.*315G>T
ENST00000682887.1:c.1710G>T	ENSP00000506946.1:n.1710G>T
ENST00000683302.1:c.1240G>T	ENSP00000507885.1:p.Glu414Ter
ENST00000683557.1:c.*141G>T	ENSP00000508029.1:n.*141G>T
ENST00000367282.6:c.1309G>T MANE Select	ENSP00000356251.4:p.Glu437Ter
ENST00000367282.5:c.1309G>T	ENSP00000356251.4:p.Glu437Ter
NM_004767.3:c.1309G>T	NP_004758.3:p.Glu437Ter
XM_011510158.1:c.748G>T	XP_011508460.1:p.Glu250Ter
NM_004767.4:c.1309G>T	NP_004758.3:p.Glu437Ter
XM_011510158.2:c.748G>T	XP_011508460.1:p.Glu250Ter
NM_004767.5:c.1309G>T MANE Select	NP_004758.3:p.Glu437Ter