Canonical Allele Identifier: CA344235968

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097470T>C (hg19) ; chr1:g.202128342T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128342T>C , CM000663.2:g.202128342T>C	GRCh38
NC_000001.10:g.202097470T>C , CM000663.1:g.202097470T>C	GRCh37
NC_000001.9:g.200364093T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.813T>C
ENST00000682545.1:c.*238T>C	ENSP00000508402.1:n.*238T>C
ENST00000682887.1:c.1633T>C	ENSP00000506946.1:n.1633T>C
ENST00000683302.1:c.1163T>C	ENSP00000507885.1:p.Ile388Thr
ENST00000683557.1:c.*64T>C	ENSP00000508029.1:n.*64T>C
ENST00000367282.6:c.1232T>C MANE Select	ENSP00000356251.4:p.Ile411Thr
ENST00000367282.5:c.1232T>C	ENSP00000356251.4:p.Ile411Thr
NM_004767.3:c.1232T>C	NP_004758.3:p.Ile411Thr
XM_011510158.1:c.671T>C	XP_011508460.1:p.Ile224Thr
NM_004767.4:c.1232T>C	NP_004758.3:p.Ile411Thr
XM_011510158.2:c.671T>C	XP_011508460.1:p.Ile224Thr
NM_004767.5:c.1232T>C MANE Select	NP_004758.3:p.Ile411Thr