Canonical Allele Identifier: CA344235984

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097479T>C (hg19) ; chr1:g.202128351T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128351T>C , CM000663.2:g.202128351T>C	GRCh38
NC_000001.10:g.202097479T>C , CM000663.1:g.202097479T>C	GRCh37
NC_000001.9:g.200364102T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.822T>C
ENST00000682545.1:c.*247T>C	ENSP00000508402.1:n.*247T>C
ENST00000682887.1:c.1642T>C	ENSP00000506946.1:n.1642T>C
ENST00000683302.1:c.1172T>C	ENSP00000507885.1:p.Val391Ala
ENST00000683557.1:c.*73T>C	ENSP00000508029.1:n.*73T>C
ENST00000367282.6:c.1241T>C MANE Select	ENSP00000356251.4:p.Val414Ala
ENST00000367282.5:c.1241T>C	ENSP00000356251.4:p.Val414Ala
NM_004767.3:c.1241T>C	NP_004758.3:p.Val414Ala
XM_011510158.1:c.680T>C	XP_011508460.1:p.Val227Ala
NM_004767.4:c.1241T>C	NP_004758.3:p.Val414Ala
XM_011510158.2:c.680T>C	XP_011508460.1:p.Val227Ala
NM_004767.5:c.1241T>C MANE Select	NP_004758.3:p.Val414Ala