Canonical Allele Identifier: CA1562859324

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692769T= , CM000667.2:g.90692769T=	GRCh38
NC_000005.9:g.89988586T= , CM000667.1:g.89988586T=	GRCh37
NC_000005.8:g.90024342T=	NCBI36
NG_007083.1:g.138970T=
NG_007083.2:g.168426T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7116T= MANE Select	ENSP00000384582.2:p.Asn2372=
ENST00000639431.1:c.265+16560T=	ENSP00000491057.1:n.265+16560T=
ENST00000639473.1:n.2575T=
ENST00000640012.1:c.923T=
ENST00000640374.1:n.260T=
ENST00000640403.1:c.4407T=	ENSP00000492531.1:p.Asn1469=
ENST00000640779.1:c.1845T=
ENST00000405460.6:c.7116T=	ENSP00000384582.2:p.Asn2372=
NM_032119.3:c.7116T=	NP_115495.3:p.Asn2372=
NR_003149.1:n.7129T=
XM_011543675.1:c.7113T=	XP_011541977.1:p.Asn2371=
XM_011543676.1:c.7035T=	XP_011541978.1:p.Asn2345=
XM_011543677.1:c.4419T=	XP_011541979.1:p.Asn1473=
XM_011543678.1:c.7116T=	XP_011541980.1:p.Asn2372=
XM_011543679.1:c.7116T=	XP_011541981.1:p.Asn2372=
NM_032119.4:c.7116T= MANE Select	NP_115495.3:p.Asn2372=
XM_017009963.2:c.7116T=	XP_016865452.1:p.Asn2372=
XM_017009964.2:c.7113T=	XP_016865453.1:p.Asn2371=
XM_017009965.1:c.7113T=	XP_016865454.1:p.Asn2371=
XM_017009966.2:c.7035T=	XP_016865455.1:p.Asn2345=
XM_017009967.1:c.7020T=	XP_016865456.1:p.Asn2340=
XM_017009968.2:c.7116T=	XP_016865457.1:p.Asn2372=
XM_017009969.2:c.7116T=	XP_016865458.1:p.Asn2372=
XM_017009970.2:c.7116T=	XP_016865459.1:p.Asn2372=
XM_017009971.2:c.7116T=	XP_016865460.1:p.Asn2372=
XM_017009972.1:c.234T=	XP_016865461.1:p.Asn78=
XM_017009973.1:c.234T=	XP_016865462.1:p.Asn78=
XM_017009974.2:c.7116T=	XP_016865463.1:p.Asn2372=
NR_003149.2:n.7132T=