Canonical Allele Identifier: CA422796313

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097417C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128289C>G , CM000663.2:g.202128289C>G	GRCh38
NC_000001.10:g.202097417C>G , CM000663.1:g.202097417C>G	GRCh37
NC_000001.9:g.200364040C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.760C>G
ENST00000682545.1:c.*185C>G	ENSP00000508402.1:n.*185C>G
ENST00000682887.1:c.1580C>G	ENSP00000506946.1:n.1580C>G
ENST00000683302.1:c.1110C>G	ENSP00000507885.1:p.Thr370=
ENST00000683557.1:c.*11C>G	ENSP00000508029.1:n.*11C>G
ENST00000367282.6:c.1179C>G MANE Select	ENSP00000356251.4:p.Thr393=
ENST00000367282.5:c.1179C>G	ENSP00000356251.4:p.Thr393=
NM_004767.3:c.1179C>G	NP_004758.3:p.Thr393=
XM_011510158.1:c.618C>G	XP_011508460.1:p.Thr206=
NM_004767.4:c.1179C>G	NP_004758.3:p.Thr393=
XM_011510158.2:c.618C>G	XP_011508460.1:p.Thr206=
NM_004767.5:c.1179C>G MANE Select	NP_004758.3:p.Thr393=