Canonical Allele Identifier: CA1562836903

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644782A= , CM000667.2:g.90644782A=	GRCh38
NC_000005.9:g.89940599A= , CM000667.1:g.89940599A=	GRCh37
NC_000005.8:g.89976355A=	NCBI36
NG_007083.1:g.90983A=
NG_007083.2:g.120439A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2811A= MANE Select	ENSP00000384582.2:p.Thr937=
ENST00000504142.2:n.1577A=
ENST00000639676.1:n.409A=
ENST00000640403.1:c.114A=	ENSP00000492531.1:p.Thr38=
ENST00000405460.6:c.2811A=	ENSP00000384582.2:p.Thr937=
ENST00000504142.1:c.1576A=
NM_032119.3:c.2811A=	NP_115495.3:p.Thr937=
NR_003149.1:n.2907A=
XM_011543675.1:c.2811A=	XP_011541977.1:p.Thr937=
XM_011543676.1:c.2811A=	XP_011541978.1:p.Thr937=
XM_011543677.1:c.114A=	XP_011541979.1:p.Thr38=
XM_011543678.1:c.2811A=	XP_011541980.1:p.Thr937=
XM_011543679.1:c.2811A=	XP_011541981.1:p.Thr937=
NM_032119.4:c.2811A= MANE Select	NP_115495.3:p.Thr937=
XM_017009963.2:c.2811A=	XP_016865452.1:p.Thr937=
XM_017009964.2:c.2811A=	XP_016865453.1:p.Thr937=
XM_017009965.1:c.2808A=	XP_016865454.1:p.Thr936=
XM_017009966.2:c.2811A=	XP_016865455.1:p.Thr937=
XM_017009967.1:c.2715A=	XP_016865456.1:p.Thr905=
XM_017009968.2:c.2811A=	XP_016865457.1:p.Thr937=
XM_017009969.2:c.2811A=	XP_016865458.1:p.Thr937=
XM_017009970.2:c.2811A=	XP_016865459.1:p.Thr937=
XM_017009971.2:c.2811A=	XP_016865460.1:p.Thr937=
XM_017009974.2:c.2811A=	XP_016865463.1:p.Thr937=
NR_003149.2:n.2910A=