Canonical Allele Identifier: CA35471437

Gene: GPR37L1

Linked Data

• dbSNP Id: rs145269048
• gnomAD v4: 1-202128321-C-T
• MyVariant Identifiers: chr1:g.202097449C>T (hg19) ; chr1:g.202128321C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128321C>T , CM000663.2:g.202128321C>T	GRCh38
NC_000001.10:g.202097449C>T , CM000663.1:g.202097449C>T	GRCh37
NC_000001.9:g.200364072C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.792C>T
ENST00000682545.1:c.*217C>T	ENSP00000508402.1:n.*217C>T
ENST00000682887.1:c.1612C>T	ENSP00000506946.1:n.1612C>T
ENST00000683302.1:c.1142C>T	ENSP00000507885.1:p.Ser381Phe
ENST00000683557.1:c.*43C>T	ENSP00000508029.1:n.*43C>T
ENST00000367282.6:c.1211C>T MANE Select	ENSP00000356251.4:p.Ser404Phe
ENST00000367282.5:c.1211C>T	ENSP00000356251.4:p.Ser404Phe
NM_004767.3:c.1211C>T	NP_004758.3:p.Ser404Phe
XM_011510158.1:c.650C>T	XP_011508460.1:p.Ser217Phe
NM_004767.4:c.1211C>T	NP_004758.3:p.Ser404Phe
XM_011510158.2:c.650C>T	XP_011508460.1:p.Ser217Phe
NM_004767.5:c.1211C>T MANE Select	NP_004758.3:p.Ser404Phe