Canonical Allele Identifier: CA1562875041

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90729084A= , CM000667.2:g.90729084A=	GRCh38
NC_000005.9:g.90024901A= , CM000667.1:g.90024901A=	GRCh37
NC_000005.8:g.90060657A=	NCBI36
NG_007083.1:g.175285A=
NG_007083.2:g.204741A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10426+151A= MANE Select	ENSP00000384582.2:n.10426+151A=
ENST00000639431.1:c.265+52875A=	ENSP00000491057.1:n.265+52875A=
ENST00000640374.1:n.3570+151A=
ENST00000640464.1:n.845+151A=
ENST00000405460.6:c.10426+151A=	ENSP00000384582.2:n.10426+151A=
ENST00000509621.1:c.3123+151A=
NM_032119.3:c.10426+151A=	NP_115495.3:n.10426+151A=
NR_003149.1:n.10439+151A=
XM_011543675.1:c.10423+151A=	XP_011541977.1:n.10423+151A=
XM_011543676.1:c.10345+151A=	XP_011541978.1:n.10345+151A=
XM_011543677.1:c.7729+151A=	XP_011541979.1:n.7729+151A=
XM_011543678.1:c.10426+151A=	XP_011541980.1:n.10426+151A=
XM_011543679.1:c.10426+151A=	XP_011541981.1:n.10426+151A=
XR_948560.1:n.271+11823T=
NM_032119.4:c.10426+151A= MANE Select	NP_115495.3:n.10426+151A=
XM_017009963.2:c.10447+151A=	XP_016865452.1:n.10447+151A=
XM_017009964.2:c.10444+151A=	XP_016865453.1:n.10444+151A=
XM_017009965.1:c.10444+151A=	XP_016865454.1:n.10444+151A=
XM_017009966.2:c.10366+151A=	XP_016865455.1:n.10366+151A=
XM_017009967.1:c.10351+151A=	XP_016865456.1:n.10351+151A=
XM_017009968.2:c.10447+151A=	XP_016865457.1:n.10447+151A=
XM_017009969.2:c.10447+151A=	XP_016865458.1:n.10447+151A=
XM_017009970.2:c.10447+151A=	XP_016865459.1:n.10447+151A=
XM_017009971.2:c.10447+151A=	XP_016865460.1:n.10447+151A=
XM_017009972.1:c.3565+151A=	XP_016865461.1:n.3565+151A=
XM_017009973.1:c.3544+151A=	XP_016865462.1:n.3544+151A=
XM_017009974.2:c.10447+151A=	XP_016865463.1:n.10447+151A=
XR_001742802.1:n.2522+11823T=
NR_003149.2:n.10442+151A=