Canonical Allele Identifier: CA1562869767

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720076C= , CM000667.2:g.90720076C=	GRCh38
NC_000005.9:g.90015893C= , CM000667.1:g.90015893C=	GRCh37
NC_000005.8:g.90051649C=	NCBI36
NG_007083.1:g.166277C=
NG_007083.2:g.195733C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9476C= MANE Select	NP_115495.3:p.Thr3159=
ENST00000405460.9:c.9476C= MANE Select	ENSP00000384582.2:p.Thr3159=
NM_032119.3:c.9476C=	NP_115495.3:p.Thr3159=
NR_003149.1:n.9489C=
NR_003149.2:n.9492C=
ENST00000405460.6:c.9476C=	ENSP00000384582.2:p.Thr3159=
ENST00000509621.1:c.2173C=
ENST00000639431.1:c.265+43867C=	ENSP00000491057.1:n.265+43867C=
ENST00000640374.1:n.2620C=
ENST00000640779.1:c.4205C=
XM_011543675.1:c.9473C=	XP_011541977.1:p.Thr3158=
XM_011543676.1:c.9395C=	XP_011541978.1:p.Thr3132=
XM_011543677.1:c.6779C=	XP_011541979.1:p.Thr2260=
XM_011543678.1:c.9476C=	XP_011541980.1:p.Thr3159=
XM_011543679.1:c.9476C=	XP_011541981.1:p.Thr3159=
XM_017009963.2:c.9497C=	XP_016865452.1:p.Thr3166=
XM_017009964.2:c.9494C=	XP_016865453.1:p.Thr3165=
XM_017009965.1:c.9494C=	XP_016865454.1:p.Thr3165=
XM_017009966.2:c.9416C=	XP_016865455.1:p.Thr3139=
XM_017009967.1:c.9401C=	XP_016865456.1:p.Thr3134=
XM_017009968.2:c.9497C=	XP_016865457.1:p.Thr3166=
XM_017009969.2:c.9497C=	XP_016865458.1:p.Thr3166=
XM_017009970.2:c.9497C=	XP_016865459.1:p.Thr3166=
XM_017009971.2:c.9497C=	XP_016865460.1:p.Thr3166=
XM_017009972.1:c.2615C=	XP_016865461.1:p.Thr872=
XM_017009973.1:c.2594C=	XP_016865462.1:p.Thr865=
XM_017009974.2:c.9497C=	XP_016865463.1:p.Thr3166=
XR_001742802.1:n.2523-4267G=
XR_948560.1:n.272-4267G=