Canonical Allele Identifier: CA1562859255

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692632T= , CM000667.2:g.90692632T=	GRCh38
NC_000005.9:g.89988449T= , CM000667.1:g.89988449T=	GRCh37
NC_000005.8:g.90024205T=	NCBI36
NG_007083.1:g.138833T=
NG_007083.2:g.168289T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6979T= MANE Select	ENSP00000384582.2:p.Ser2327=
ENST00000639431.1:c.265+16423T=	ENSP00000491057.1:n.265+16423T=
ENST00000639473.1:n.2438T=
ENST00000640012.1:c.786T=
ENST00000640374.1:n.123T=
ENST00000640403.1:c.4270T=	ENSP00000492531.1:p.Ser1424=
ENST00000640779.1:c.1708T=
ENST00000405460.6:c.6979T=	ENSP00000384582.2:p.Ser2327=
NM_032119.3:c.6979T=	NP_115495.3:p.Ser2327=
NR_003149.1:n.6992T=
XM_011543675.1:c.6976T=	XP_011541977.1:p.Ser2326=
XM_011543676.1:c.6898T=	XP_011541978.1:p.Ser2300=
XM_011543677.1:c.4282T=	XP_011541979.1:p.Ser1428=
XM_011543678.1:c.6979T=	XP_011541980.1:p.Ser2327=
XM_011543679.1:c.6979T=	XP_011541981.1:p.Ser2327=
NM_032119.4:c.6979T= MANE Select	NP_115495.3:p.Ser2327=
XM_017009963.2:c.6979T=	XP_016865452.1:p.Ser2327=
XM_017009964.2:c.6976T=	XP_016865453.1:p.Ser2326=
XM_017009965.1:c.6976T=	XP_016865454.1:p.Ser2326=
XM_017009966.2:c.6898T=	XP_016865455.1:p.Ser2300=
XM_017009967.1:c.6883T=	XP_016865456.1:p.Ser2295=
XM_017009968.2:c.6979T=	XP_016865457.1:p.Ser2327=
XM_017009969.2:c.6979T=	XP_016865458.1:p.Ser2327=
XM_017009970.2:c.6979T=	XP_016865459.1:p.Ser2327=
XM_017009971.2:c.6979T=	XP_016865460.1:p.Ser2327=
XM_017009972.1:c.97T=	XP_016865461.1:p.Ser33=
XM_017009973.1:c.97T=	XP_016865462.1:p.Ser33=
XM_017009974.2:c.6979T=	XP_016865463.1:p.Ser2327=
NR_003149.2:n.6995T=