Canonical Allele Identifier: CA360409090

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810621G>A , CM000667.2:g.90810621G>A	GRCh38
NC_000005.9:g.90106438G>A , CM000667.1:g.90106438G>A	GRCh37
NC_000005.8:g.90142194G>A	NCBI36
NG_007083.1:g.256822G>A
NG_007083.2:g.286278G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15361G>A MANE Select	NP_115495.3:p.Val5121Met
ENST00000405460.9:c.15361G>A MANE Select	ENSP00000384582.2:p.Val5121Met
NM_032119.3:c.15361G>A	NP_115495.3:p.Val5121Met
NR_003149.1:n.15374G>A
NR_003149.2:n.15377G>A
ENST00000405460.6:c.15361G>A	ENSP00000384582.2:p.Val5121Met
ENST00000425867.2:c.2344G>A	ENSP00000392618.2:p.Val782Met
ENST00000425867.3:c.4315G>A	ENSP00000392618.3:p.Val1439Met
ENST00000638510.1:n.2628G>A
ENST00000639431.1:c.265+134412G>A	ENSP00000491057.1:n.265+134412G>A
ENST00000640407.1:c.1771G>A	ENSP00000491425.1:p.Val591Met
XM_011543675.1:c.15358G>A	XP_011541977.1:p.Val5120Met
XM_011543676.1:c.15280G>A	XP_011541978.1:p.Val5094Met
XM_011543677.1:c.12664G>A	XP_011541979.1:p.Val4222Met
XM_017009963.2:c.15382G>A	XP_016865452.1:p.Val5128Met
XM_017009964.2:c.15379G>A	XP_016865453.1:p.Val5127Met
XM_017009965.1:c.15379G>A	XP_016865454.1:p.Val5127Met
XM_017009966.2:c.15301G>A	XP_016865455.1:p.Val5101Met
XM_017009967.1:c.15286G>A	XP_016865456.1:p.Val5096Met
XM_017009968.2:c.15202G>A	XP_016865457.1:p.Val5068Met
XM_017009969.2:c.15382G>A	XP_016865458.1:p.Val5128Met
XM_017009971.2:c.*315G>A	XP_016865460.1:n.*315G>A
XM_017009972.1:c.8500G>A	XP_016865461.1:p.Val2834Met
XM_017009973.1:c.8479G>A	XP_016865462.1:p.Val2827Met