Canonical Allele Identifier: CA122810752

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90855829G>A , CM000667.2:g.90855829G>A	GRCh38
NC_000005.9:g.90151646G>A , CM000667.1:g.90151646G>A	GRCh37
NC_000005.8:g.90187402G>A	NCBI36
NG_007083.1:g.302030G>A
NG_007083.2:g.331486G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.17683G>A MANE Select	ENSP00000384582.2:p.Val5895Ile
ENST00000425867.3:c.6637G>A	ENSP00000392618.3:p.Val2213Ile
ENST00000638510.1:n.4950G>A
ENST00000638990.1:c.895G>A
ENST00000639431.1:c.266-129515G>A	ENSP00000491057.1:n.266-129515G>A
ENST00000640407.1:c.4132G>A	ENSP00000491425.1:n.4132G>A
ENST00000405460.6:c.17683G>A	ENSP00000384582.2:p.Val5895Ile
ENST00000425867.2:c.4666G>A	ENSP00000392618.2:p.Val1556Ile
ENST00000503852.1:n.231G>A
NM_032119.3:c.17683G>A	NP_115495.3:p.Val5895Ile
NR_003149.1:n.17696G>A
XM_011543675.1:c.17680G>A	XP_011541977.1:p.Val5894Ile
XM_011543676.1:c.17602G>A	XP_011541978.1:p.Val5868Ile
XM_011543677.1:c.14986G>A	XP_011541979.1:p.Val4996Ile
NM_032119.4:c.17683G>A MANE Select	NP_115495.3:p.Val5895Ile
XM_017009963.2:c.17704G>A	XP_016865452.1:p.Val5902Ile
XM_017009964.2:c.17701G>A	XP_016865453.1:p.Val5901Ile
XM_017009965.1:c.17701G>A	XP_016865454.1:p.Val5901Ile
XM_017009966.2:c.17623G>A	XP_016865455.1:p.Val5875Ile
XM_017009967.1:c.17608G>A	XP_016865456.1:p.Val5870Ile
XM_017009968.2:c.17524G>A	XP_016865457.1:p.Val5842Ile
XM_017009969.2:c.17704G>A	XP_016865458.1:p.Val5902Ile
XM_017009972.1:c.10822G>A	XP_016865461.1:p.Val3608Ile
XM_017009973.1:c.10801G>A	XP_016865462.1:p.Val3601Ile
NR_003149.2:n.17699G>A