Canonical Allele Identifier: CA1220026671

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128383C= , CM000663.2:g.202128383C=	GRCh38
NC_000001.10:g.202097511C= , CM000663.1:g.202097511C=	GRCh37
NC_000001.9:g.200364134C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.854C=
ENST00000682545.1:c.*279C=	ENSP00000508402.1:n.*279C=
ENST00000682887.1:c.1674C=	ENSP00000506946.1:n.1674C=
ENST00000683302.1:c.1204C=	ENSP00000507885.1:p.Gln402=
ENST00000683557.1:c.*105C=	ENSP00000508029.1:n.*105C=
ENST00000367282.6:c.1273C= MANE Select	ENSP00000356251.4:p.Gln425=
ENST00000367282.5:c.1273C=	ENSP00000356251.4:p.Gln425=
NM_004767.3:c.1273C=	NP_004758.3:p.Gln425=
XM_011510158.1:c.712C=	XP_011508460.1:p.Gln238=
NM_004767.4:c.1273C=	NP_004758.3:p.Gln425=
XM_011510158.2:c.712C=	XP_011508460.1:p.Gln238=
NM_004767.5:c.1273C= MANE Select	NP_004758.3:p.Gln425=