Canonical Allele Identifier: CA1562869782

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720082C= , CM000667.2:g.90720082C=	GRCh38
NC_000005.9:g.90015899C= , CM000667.1:g.90015899C=	GRCh37
NC_000005.8:g.90051655C=	NCBI36
NG_007083.1:g.166283C=
NG_007083.2:g.195739C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9482C= MANE Select	NP_115495.3:p.Pro3161=
ENST00000405460.9:c.9482C= MANE Select	ENSP00000384582.2:p.Pro3161=
NM_032119.3:c.9482C=	NP_115495.3:p.Pro3161=
NR_003149.1:n.9495C=
NR_003149.2:n.9498C=
ENST00000405460.6:c.9482C=	ENSP00000384582.2:p.Pro3161=
ENST00000509621.1:c.2179C=
ENST00000639431.1:c.265+43873C=	ENSP00000491057.1:n.265+43873C=
ENST00000640374.1:n.2626C=
ENST00000640779.1:c.4211C=
XM_011543675.1:c.9479C=	XP_011541977.1:p.Pro3160=
XM_011543676.1:c.9401C=	XP_011541978.1:p.Pro3134=
XM_011543677.1:c.6785C=	XP_011541979.1:p.Pro2262=
XM_011543678.1:c.9482C=	XP_011541980.1:p.Pro3161=
XM_011543679.1:c.9482C=	XP_011541981.1:p.Pro3161=
XM_017009963.2:c.9503C=	XP_016865452.1:p.Pro3168=
XM_017009964.2:c.9500C=	XP_016865453.1:p.Pro3167=
XM_017009965.1:c.9500C=	XP_016865454.1:p.Pro3167=
XM_017009966.2:c.9422C=	XP_016865455.1:p.Pro3141=
XM_017009967.1:c.9407C=	XP_016865456.1:p.Pro3136=
XM_017009968.2:c.9503C=	XP_016865457.1:p.Pro3168=
XM_017009969.2:c.9503C=	XP_016865458.1:p.Pro3168=
XM_017009970.2:c.9503C=	XP_016865459.1:p.Pro3168=
XM_017009971.2:c.9503C=	XP_016865460.1:p.Pro3168=
XM_017009972.1:c.2621C=	XP_016865461.1:p.Pro874=
XM_017009973.1:c.2600C=	XP_016865462.1:p.Pro867=
XM_017009974.2:c.9503C=	XP_016865463.1:p.Pro3168=
XR_001742802.1:n.2523-4273G=
XR_948560.1:n.272-4273G=