Canonical Allele Identifier: CA445403417

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90685793A>T , CM000667.2:g.90685793A>T	GRCh38
NC_000005.9:g.89981610A>T , CM000667.1:g.89981610A>T	GRCh37
NC_000005.8:g.90017366A>T	NCBI36
NG_007083.1:g.131994A>T
NG_007083.2:g.161450A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.6288A>T MANE Select	NP_115495.3:p.Pro2096=
ENST00000405460.9:c.6288A>T MANE Select	ENSP00000384582.2:p.Pro2096=
NM_032119.3:c.6288A>T	NP_115495.3:p.Pro2096=
NR_003149.1:n.6384A>T
NR_003149.2:n.6387A>T
ENST00000405460.6:c.6288A>T	ENSP00000384582.2:p.Pro2096=
ENST00000639431.1:c.265+9584A>T	ENSP00000491057.1:n.265+9584A>T
ENST00000639473.1:n.1747A>T
ENST00000640012.1:c.178A>T
ENST00000640403.1:c.3579A>T	ENSP00000492531.1:p.Pro1193=
ENST00000640779.1:c.1100A>T
XM_011543675.1:c.6285A>T	XP_011541977.1:p.Pro2095=
XM_011543676.1:c.6207A>T	XP_011541978.1:p.Pro2069=
XM_011543677.1:c.3591A>T	XP_011541979.1:p.Pro1197=
XM_011543678.1:c.6288A>T	XP_011541980.1:p.Pro2096=
XM_011543679.1:c.6288A>T	XP_011541981.1:p.Pro2096=
XM_017009963.2:c.6288A>T	XP_016865452.1:p.Pro2096=
XM_017009964.2:c.6285A>T	XP_016865453.1:p.Pro2095=
XM_017009965.1:c.6285A>T	XP_016865454.1:p.Pro2095=
XM_017009966.2:c.6207A>T	XP_016865455.1:p.Pro2069=
XM_017009967.1:c.6192A>T	XP_016865456.1:p.Pro2064=
XM_017009968.2:c.6288A>T	XP_016865457.1:p.Pro2096=
XM_017009969.2:c.6288A>T	XP_016865458.1:p.Pro2096=
XM_017009970.2:c.6288A>T	XP_016865459.1:p.Pro2096=
XM_017009971.2:c.6288A>T	XP_016865460.1:p.Pro2096=
XM_017009973.1:c.-512A>T	XP_016865462.1:n.-512A>T
XM_017009974.2:c.6288A>T	XP_016865463.1:p.Pro2096=