Canonical Allele Identifier: CA344235918

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097446T>C (hg19) ; chr1:g.202128318T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128318T>C , CM000663.2:g.202128318T>C	GRCh38
NC_000001.10:g.202097446T>C , CM000663.1:g.202097446T>C	GRCh37
NC_000001.9:g.200364069T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.789T>C
ENST00000682545.1:c.*214T>C	ENSP00000508402.1:n.*214T>C
ENST00000682887.1:c.1609T>C	ENSP00000506946.1:n.1609T>C
ENST00000683302.1:c.1139T>C	ENSP00000507885.1:p.Phe380Ser
ENST00000683557.1:c.*40T>C	ENSP00000508029.1:n.*40T>C
ENST00000367282.6:c.1208T>C MANE Select	ENSP00000356251.4:p.Phe403Ser
ENST00000367282.5:c.1208T>C	ENSP00000356251.4:p.Phe403Ser
NM_004767.3:c.1208T>C	NP_004758.3:p.Phe403Ser
XM_011510158.1:c.647T>C	XP_011508460.1:p.Phe216Ser
NM_004767.4:c.1208T>C	NP_004758.3:p.Phe403Ser
XM_011510158.2:c.647T>C	XP_011508460.1:p.Phe216Ser
NM_004767.5:c.1208T>C MANE Select	NP_004758.3:p.Phe403Ser