Canonical Allele Identifier: CA3341846

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90807738G>T , CM000667.2:g.90807738G>T	GRCh38
NC_000005.9:g.90103555G>T , CM000667.1:g.90103555G>T	GRCh37
NC_000005.8:g.90139311G>T	NCBI36
NG_007083.1:g.253939G>T
NG_007083.2:g.283395G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14972+1G>T MANE Select	NP_115495.3:n.14972+1G>T
ENST00000405460.9:c.14972+1G>T MANE Select	ENSP00000384582.2:n.14972+1G>T
NM_032119.3:c.14972+1G>T	NP_115495.3:n.14972+1G>T
NR_003149.1:n.14985+1G>T
NR_003149.2:n.14988+1G>T
ENST00000405460.6:c.14972+1G>T	ENSP00000384582.2:n.14972+1G>T
ENST00000425867.2:c.1955+1G>T	ENSP00000392618.2:n.1955+1G>T
ENST00000425867.3:c.3926+1G>T	ENSP00000392618.3:n.3926+1G>T
ENST00000638510.1:n.2239+1G>T
ENST00000638585.1:n.428-2495G>T
ENST00000639431.1:c.265+131529G>T	ENSP00000491057.1:n.265+131529G>T
ENST00000640407.1:c.1382+1G>T	ENSP00000491425.1:n.1382+1G>T
XM_011543675.1:c.14969+1G>T	XP_011541977.1:n.14969+1G>T
XM_011543676.1:c.14891+1G>T	XP_011541978.1:n.14891+1G>T
XM_011543677.1:c.12275+1G>T	XP_011541979.1:n.12275+1G>T
XM_011543678.1:c.14972+1G>T	XP_011541980.1:n.14972+1G>T
XM_017009963.2:c.14993+1G>T	XP_016865452.1:n.14993+1G>T
XM_017009964.2:c.14990+1G>T	XP_016865453.1:n.14990+1G>T
XM_017009965.1:c.14990+1G>T	XP_016865454.1:n.14990+1G>T
XM_017009966.2:c.14912+1G>T	XP_016865455.1:n.14912+1G>T
XM_017009967.1:c.14897+1G>T	XP_016865456.1:n.14897+1G>T
XM_017009968.2:c.14818+1G>T	XP_016865457.1:n.14818+1G>T
XM_017009969.2:c.14993+1G>T	XP_016865458.1:n.14993+1G>T
XM_017009970.2:c.14993+1G>T	XP_016865459.1:n.14993+1G>T
XM_017009971.2:c.14818+1G>T	XP_016865460.1:n.14818+1G>T
XM_017009972.1:c.8111+1G>T	XP_016865461.1:n.8111+1G>T
XM_017009973.1:c.8090+1G>T	XP_016865462.1:n.8090+1G>T