Canonical Allele Identifier: CA344235894

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097437T>C (hg19) ; chr1:g.202128309T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128309T>C , CM000663.2:g.202128309T>C	GRCh38
NC_000001.10:g.202097437T>C , CM000663.1:g.202097437T>C	GRCh37
NC_000001.9:g.200364060T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.780T>C
ENST00000682545.1:c.*205T>C	ENSP00000508402.1:n.*205T>C
ENST00000682887.1:c.1600T>C	ENSP00000506946.1:n.1600T>C
ENST00000683302.1:c.1130T>C	ENSP00000507885.1:p.Ile377Thr
ENST00000683557.1:c.*31T>C	ENSP00000508029.1:n.*31T>C
ENST00000367282.6:c.1199T>C MANE Select	ENSP00000356251.4:p.Ile400Thr
ENST00000367282.5:c.1199T>C	ENSP00000356251.4:p.Ile400Thr
NM_004767.3:c.1199T>C	NP_004758.3:p.Ile400Thr
XM_011510158.1:c.638T>C	XP_011508460.1:p.Ile213Thr
NM_004767.4:c.1199T>C	NP_004758.3:p.Ile400Thr
XM_011510158.2:c.638T>C	XP_011508460.1:p.Ile213Thr
NM_004767.5:c.1199T>C MANE Select	NP_004758.3:p.Ile400Thr