Canonical Allele Identifier: CA1144065896

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128334G= , CM000663.2:g.202128334G=	GRCh38
NC_000001.10:g.202097462G= , CM000663.1:g.202097462G=	GRCh37
NC_000001.9:g.200364085G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.805G=
ENST00000682545.1:c.*230G=	ENSP00000508402.1:n.*230G=
ENST00000682887.1:c.1625G=	ENSP00000506946.1:n.1625G=
ENST00000683302.1:c.1155G=	ENSP00000507885.1:p.Lys385=
ENST00000683557.1:c.*56G=	ENSP00000508029.1:n.*56G=
ENST00000367282.6:c.1224G= MANE Select	ENSP00000356251.4:p.Lys408=
ENST00000367282.5:c.1224G=	ENSP00000356251.4:p.Lys408=
NM_004767.3:c.1224G=	NP_004758.3:p.Lys408=
XM_011510158.1:c.663G=	XP_011508460.1:p.Lys221=
NM_004767.4:c.1224G=	NP_004758.3:p.Lys408=
XM_011510158.2:c.663G=	XP_011508460.1:p.Lys221=
NM_004767.5:c.1224G= MANE Select	NP_004758.3:p.Lys408=