Canonical Allele Identifier: CA1562873566

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725622T= , CM000667.2:g.90725622T=	GRCh38
NC_000005.9:g.90021439T= , CM000667.1:g.90021439T=	GRCh37
NC_000005.8:g.90057195T=	NCBI36
NG_007083.1:g.171823T=
NG_007083.2:g.201279T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10127T= MANE Select	ENSP00000384582.2:p.Ile3376=
ENST00000639431.1:c.265+49413T=	ENSP00000491057.1:n.265+49413T=
ENST00000640374.1:n.3271T=
ENST00000640464.1:n.546T=
ENST00000405460.6:c.10127T=	ENSP00000384582.2:p.Ile3376=
ENST00000509621.1:c.2824T=
NM_032119.3:c.10127T=	NP_115495.3:p.Ile3376=
NR_003149.1:n.10140T=
XM_011543675.1:c.10124T=	XP_011541977.1:p.Ile3375=
XM_011543676.1:c.10046T=	XP_011541978.1:p.Ile3349=
XM_011543677.1:c.7430T=	XP_011541979.1:p.Ile2477=
XM_011543678.1:c.10127T=	XP_011541980.1:p.Ile3376=
XM_011543679.1:c.10127T=	XP_011541981.1:p.Ile3376=
XR_948560.1:n.272-9813A=
NM_032119.4:c.10127T= MANE Select	NP_115495.3:p.Ile3376=
XM_017009963.2:c.10148T=	XP_016865452.1:p.Ile3383=
XM_017009964.2:c.10145T=	XP_016865453.1:p.Ile3382=
XM_017009965.1:c.10145T=	XP_016865454.1:p.Ile3382=
XM_017009966.2:c.10067T=	XP_016865455.1:p.Ile3356=
XM_017009967.1:c.10052T=	XP_016865456.1:p.Ile3351=
XM_017009968.2:c.10148T=	XP_016865457.1:p.Ile3383=
XM_017009969.2:c.10148T=	XP_016865458.1:p.Ile3383=
XM_017009970.2:c.10148T=	XP_016865459.1:p.Ile3383=
XM_017009971.2:c.10148T=	XP_016865460.1:p.Ile3383=
XM_017009972.1:c.3266T=	XP_016865461.1:p.Ile1089=
XM_017009973.1:c.3245T=	XP_016865462.1:p.Ile1082=
XM_017009974.2:c.10148T=	XP_016865463.1:p.Ile3383=
XR_001742802.1:n.2523-9813A=
NR_003149.2:n.10143T=