Canonical Allele Identifier: CA360427563

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90829187G>A , CM000667.2:g.90829187G>A	GRCh38
NC_000005.9:g.90125004G>A , CM000667.1:g.90125004G>A	GRCh37
NC_000005.8:g.90160760G>A	NCBI36
NG_007083.1:g.275388G>A
NG_007083.2:g.304844G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16611+1G>A MANE Select	NP_115495.3:n.16611+1G>A
ENST00000405460.9:c.16611+1G>A MANE Select	ENSP00000384582.2:n.16611+1G>A
NM_032119.3:c.16611+1G>A	NP_115495.3:n.16611+1G>A
NR_003149.1:n.16624+1G>A
NR_003149.2:n.16627+1G>A
ENST00000405460.6:c.16611+1G>A	ENSP00000384582.2:n.16611+1G>A
ENST00000425867.2:c.3594+1G>A	ENSP00000392618.2:n.3594+1G>A
ENST00000425867.3:c.5565+1G>A	ENSP00000392618.3:n.5565+1G>A
ENST00000638510.1:n.3878+1G>A
ENST00000639431.1:c.265+152978G>A	ENSP00000491057.1:n.265+152978G>A
ENST00000640061.1:n.128+7005G>A
ENST00000640407.1:c.3060+1G>A	ENSP00000491425.1:n.3060+1G>A
XM_011543675.1:c.16608+1G>A	XP_011541977.1:n.16608+1G>A
XM_011543676.1:c.16530+1G>A	XP_011541978.1:n.16530+1G>A
XM_011543677.1:c.13914+1G>A	XP_011541979.1:n.13914+1G>A
XM_017009963.2:c.16632+1G>A	XP_016865452.1:n.16632+1G>A
XM_017009964.2:c.16629+1G>A	XP_016865453.1:n.16629+1G>A
XM_017009965.1:c.16629+1G>A	XP_016865454.1:n.16629+1G>A
XM_017009966.2:c.16551+1G>A	XP_016865455.1:n.16551+1G>A
XM_017009967.1:c.16536+1G>A	XP_016865456.1:n.16536+1G>A
XM_017009968.2:c.16452+1G>A	XP_016865457.1:n.16452+1G>A
XM_017009969.2:c.16632+1G>A	XP_016865458.1:n.16632+1G>A
XM_017009972.1:c.9750+1G>A	XP_016865461.1:n.9750+1G>A
XM_017009973.1:c.9729+1G>A	XP_016865462.1:n.9729+1G>A