Canonical Allele Identifier: CA1144199199

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128370C= , CM000663.2:g.202128370C=	GRCh38
NC_000001.10:g.202097498C= , CM000663.1:g.202097498C=	GRCh37
NC_000001.9:g.200364121C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.841C=
ENST00000682545.1:c.*266C=	ENSP00000508402.1:n.*266C=
ENST00000682887.1:c.1661C=	ENSP00000506946.1:n.1661C=
ENST00000683302.1:c.1191C=	ENSP00000507885.1:p.Cys397=
ENST00000683557.1:c.*92C=	ENSP00000508029.1:n.*92C=
ENST00000367282.6:c.1260C= MANE Select	ENSP00000356251.4:p.Cys420=
ENST00000367282.5:c.1260C=	ENSP00000356251.4:p.Cys420=
NM_004767.3:c.1260C=	NP_004758.3:p.Cys420=
XM_011510158.1:c.699C=	XP_011508460.1:p.Cys233=
NM_004767.4:c.1260C=	NP_004758.3:p.Cys420=
XM_011510158.2:c.699C=	XP_011508460.1:p.Cys233=
NM_004767.5:c.1260C= MANE Select	NP_004758.3:p.Cys420=