Canonical Allele Identifier: CA360395766

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90711242C>A , CM000667.2:g.90711242C>A	GRCh38
NC_000005.9:g.90007059C>A , CM000667.1:g.90007059C>A	GRCh37
NC_000005.8:g.90042815C>A	NCBI36
NG_007083.1:g.157443C>A
NG_007083.2:g.186899C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8962C>A MANE Select	NP_115495.3:p.Pro2988Thr
ENST00000405460.9:c.8962C>A MANE Select	ENSP00000384582.2:p.Pro2988Thr
NM_032119.3:c.8962C>A	NP_115495.3:p.Pro2988Thr
NR_003149.1:n.8975C>A
NR_003149.2:n.8978C>A
ENST00000405460.6:c.8962C>A	ENSP00000384582.2:p.Pro2988Thr
ENST00000509621.1:c.1659C>A
ENST00000639431.1:c.265+35033C>A	ENSP00000491057.1:n.265+35033C>A
ENST00000639473.1:n.4421C>A
ENST00000640012.1:c.2769C>A
ENST00000640374.1:n.2106C>A
ENST00000640779.1:c.3691C>A
XM_011543675.1:c.8959C>A	XP_011541977.1:p.Pro2987Thr
XM_011543676.1:c.8881C>A	XP_011541978.1:p.Pro2961Thr
XM_011543677.1:c.6265C>A	XP_011541979.1:p.Pro2089Thr
XM_011543678.1:c.8962C>A	XP_011541980.1:p.Pro2988Thr
XM_011543679.1:c.8962C>A	XP_011541981.1:p.Pro2988Thr
XM_017009963.2:c.8983C>A	XP_016865452.1:p.Pro2995Thr
XM_017009964.2:c.8980C>A	XP_016865453.1:p.Pro2994Thr
XM_017009965.1:c.8980C>A	XP_016865454.1:p.Pro2994Thr
XM_017009966.2:c.8902C>A	XP_016865455.1:p.Pro2968Thr
XM_017009967.1:c.8887C>A	XP_016865456.1:p.Pro2963Thr
XM_017009968.2:c.8983C>A	XP_016865457.1:p.Pro2995Thr
XM_017009969.2:c.8983C>A	XP_016865458.1:p.Pro2995Thr
XM_017009970.2:c.8983C>A	XP_016865459.1:p.Pro2995Thr
XM_017009971.2:c.8983C>A	XP_016865460.1:p.Pro2995Thr
XM_017009972.1:c.2101C>A	XP_016865461.1:p.Pro701Thr
XM_017009973.1:c.2080C>A	XP_016865462.1:p.Pro694Thr
XM_017009974.2:c.8983C>A	XP_016865463.1:p.Pro2995Thr