Canonical Allele Identifier: CA3342411

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90855803C>A , CM000667.2:g.90855803C>A	GRCh38
NC_000005.9:g.90151620C>A , CM000667.1:g.90151620C>A	GRCh37
NC_000005.8:g.90187376C>A	NCBI36
NG_007083.1:g.302004C>A
NG_007083.2:g.331460C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17657C>A MANE Select	NP_115495.3:p.Ala5886Asp
ENST00000405460.9:c.17657C>A MANE Select	ENSP00000384582.2:p.Ala5886Asp
NM_032119.3:c.17657C>A	NP_115495.3:p.Ala5886Asp
NR_003149.1:n.17670C>A
NR_003149.2:n.17673C>A
ENST00000405460.6:c.17657C>A	ENSP00000384582.2:p.Ala5886Asp
ENST00000425867.2:c.4640C>A	ENSP00000392618.2:p.Ala1547Asp
ENST00000425867.3:c.6611C>A	ENSP00000392618.3:p.Ala2204Asp
ENST00000503852.1:n.205C>A
ENST00000638510.1:n.4924C>A
ENST00000638990.1:c.869C>A
ENST00000639431.1:c.266-129541C>A	ENSP00000491057.1:n.266-129541C>A
ENST00000640407.1:c.4106C>A	ENSP00000491425.1:n.4106C>A
XM_011543675.1:c.17654C>A	XP_011541977.1:p.Ala5885Asp
XM_011543676.1:c.17576C>A	XP_011541978.1:p.Ala5859Asp
XM_011543677.1:c.14960C>A	XP_011541979.1:p.Ala4987Asp
XM_017009963.2:c.17678C>A	XP_016865452.1:p.Ala5893Asp
XM_017009964.2:c.17675C>A	XP_016865453.1:p.Ala5892Asp
XM_017009965.1:c.17675C>A	XP_016865454.1:p.Ala5892Asp
XM_017009966.2:c.17597C>A	XP_016865455.1:p.Ala5866Asp
XM_017009967.1:c.17582C>A	XP_016865456.1:p.Ala5861Asp
XM_017009968.2:c.17498C>A	XP_016865457.1:p.Ala5833Asp
XM_017009969.2:c.17678C>A	XP_016865458.1:p.Ala5893Asp
XM_017009972.1:c.10796C>A	XP_016865461.1:p.Ala3599Asp
XM_017009973.1:c.10775C>A	XP_016865462.1:p.Ala3592Asp