Canonical Allele Identifier: CA422796442

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097489T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128361T>C , CM000663.2:g.202128361T>C	GRCh38
NC_000001.10:g.202097489T>C , CM000663.1:g.202097489T>C	GRCh37
NC_000001.9:g.200364112T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.832T>C
ENST00000682545.1:c.*257T>C	ENSP00000508402.1:n.*257T>C
ENST00000682887.1:c.1652T>C	ENSP00000506946.1:n.1652T>C
ENST00000683302.1:c.1182T>C	ENSP00000507885.1:p.Leu394=
ENST00000683557.1:c.*83T>C	ENSP00000508029.1:n.*83T>C
ENST00000367282.6:c.1251T>C MANE Select	ENSP00000356251.4:p.Leu417=
ENST00000367282.5:c.1251T>C	ENSP00000356251.4:p.Leu417=
NM_004767.3:c.1251T>C	NP_004758.3:p.Leu417=
XM_011510158.1:c.690T>C	XP_011508460.1:p.Leu230=
NM_004767.4:c.1251T>C	NP_004758.3:p.Leu417=
XM_011510158.2:c.690T>C	XP_011508460.1:p.Leu230=
NM_004767.5:c.1251T>C MANE Select	NP_004758.3:p.Leu417=