Canonical Allele Identifier: CA247443

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811097C>A , CM000667.2:g.90811097C>A	GRCh38
NC_000005.9:g.90106914C>A , CM000667.1:g.90106914C>A	GRCh37
NC_000005.8:g.90142670C>A	NCBI36
NG_007083.1:g.257298C>A
NG_007083.2:g.286754C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15837C>A MANE Select	NP_115495.3:p.Ile5279=
ENST00000405460.9:c.15837C>A MANE Select	ENSP00000384582.2:p.Ile5279=
NM_032119.3:c.15837C>A	NP_115495.3:p.Ile5279=
NR_003149.1:n.15850C>A
NR_003149.2:n.15853C>A
ENST00000405460.6:c.15837C>A	ENSP00000384582.2:p.Ile5279=
ENST00000425867.2:c.2820C>A	ENSP00000392618.2:p.Ile940=
ENST00000425867.3:c.4791C>A	ENSP00000392618.3:p.Ile1597=
ENST00000638510.1:n.3104C>A
ENST00000639431.1:c.265+134888C>A	ENSP00000491057.1:n.265+134888C>A
ENST00000640407.1:c.2247C>A	ENSP00000491425.1:p.Ile749=
XM_011543675.1:c.15834C>A	XP_011541977.1:p.Ile5278=
XM_011543676.1:c.15756C>A	XP_011541978.1:p.Ile5252=
XM_011543677.1:c.13140C>A	XP_011541979.1:p.Ile4380=
XM_017009963.2:c.15858C>A	XP_016865452.1:p.Ile5286=
XM_017009964.2:c.15855C>A	XP_016865453.1:p.Ile5285=
XM_017009965.1:c.15855C>A	XP_016865454.1:p.Ile5285=
XM_017009966.2:c.15777C>A	XP_016865455.1:p.Ile5259=
XM_017009967.1:c.15762C>A	XP_016865456.1:p.Ile5254=
XM_017009968.2:c.15678C>A	XP_016865457.1:p.Ile5226=
XM_017009969.2:c.15858C>A	XP_016865458.1:p.Ile5286=
XM_017009972.1:c.8976C>A	XP_016865461.1:p.Ile2992=
XM_017009973.1:c.8955C>A	XP_016865462.1:p.Ile2985=