Canonical Allele Identifier: CA422553949

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097543C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128415C>T , CM000663.2:g.202128415C>T	GRCh38
NC_000001.10:g.202097543C>T , CM000663.1:g.202097543C>T	GRCh37
NC_000001.9:g.200364166C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.886C>T
ENST00000682545.1:c.*311C>T	ENSP00000508402.1:n.*311C>T
ENST00000682887.1:c.1706C>T	ENSP00000506946.1:n.1706C>T
ENST00000683302.1:c.1236C>T	ENSP00000507885.1:p.Cys412=
ENST00000683557.1:c.*137C>T	ENSP00000508029.1:n.*137C>T
ENST00000367282.6:c.1305C>T MANE Select	ENSP00000356251.4:p.Cys435=
ENST00000367282.5:c.1305C>T	ENSP00000356251.4:p.Cys435=
NM_004767.3:c.1305C>T	NP_004758.3:p.Cys435=
XM_011510158.1:c.744C>T	XP_011508460.1:p.Cys248=
NM_004767.4:c.1305C>T	NP_004758.3:p.Cys435=
XM_011510158.2:c.744C>T	XP_011508460.1:p.Cys248=
NM_004767.5:c.1305C>T MANE Select	NP_004758.3:p.Cys435=