Canonical Allele Identifier: CA344236002

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097490T>A (hg19) ; chr1:g.202128362T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128362T>A , CM000663.2:g.202128362T>A	GRCh38
NC_000001.10:g.202097490T>A , CM000663.1:g.202097490T>A	GRCh37
NC_000001.9:g.200364113T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.833T>A
ENST00000682545.1:c.*258T>A	ENSP00000508402.1:n.*258T>A
ENST00000682887.1:c.1653T>A	ENSP00000506946.1:n.1653T>A
ENST00000683302.1:c.1183T>A	ENSP00000507885.1:p.Cys395Ser
ENST00000683557.1:c.*84T>A	ENSP00000508029.1:n.*84T>A
ENST00000367282.6:c.1252T>A MANE Select	ENSP00000356251.4:p.Cys418Ser
ENST00000367282.5:c.1252T>A	ENSP00000356251.4:p.Cys418Ser
NM_004767.3:c.1252T>A	NP_004758.3:p.Cys418Ser
XM_011510158.1:c.691T>A	XP_011508460.1:p.Cys231Ser
NM_004767.4:c.1252T>A	NP_004758.3:p.Cys418Ser
XM_011510158.2:c.691T>A	XP_011508460.1:p.Cys231Ser
NM_004767.5:c.1252T>A MANE Select	NP_004758.3:p.Cys418Ser