Canonical Allele Identifier: CA360431193

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90863793C>A , CM000667.2:g.90863793C>A	GRCh38
NC_000005.9:g.90159610C>A , CM000667.1:g.90159610C>A	GRCh37
NC_000005.8:g.90195366C>A	NCBI36
NG_007083.1:g.309994C>A
NG_007083.2:g.339450C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17792C>A MANE Select	NP_115495.3:p.Ala5931Asp
ENST00000405460.9:c.17792C>A MANE Select	ENSP00000384582.2:p.Ala5931Asp
NM_032119.3:c.17792C>A	NP_115495.3:p.Ala5931Asp
NR_003149.1:n.17805C>A
NR_003149.2:n.17808C>A
ENST00000405460.6:c.17792C>A	ENSP00000384582.2:p.Ala5931Asp
ENST00000425867.2:c.4775C>A	ENSP00000392618.2:p.Ala1592Asp
ENST00000425867.3:c.6746C>A	ENSP00000392618.3:p.Ala2249Asp
ENST00000503852.1:n.340C>A
ENST00000638510.1:n.5059C>A
ENST00000638990.1:c.1004C>A
ENST00000639431.1:c.266-121551C>A	ENSP00000491057.1:n.266-121551C>A
ENST00000640407.1:c.4241C>A	ENSP00000491425.1:n.4241C>A
XM_011543675.1:c.17789C>A	XP_011541977.1:p.Ala5930Asp
XM_011543676.1:c.17711C>A	XP_011541978.1:p.Ala5904Asp
XM_011543677.1:c.15095C>A	XP_011541979.1:p.Ala5032Asp
XM_017009963.2:c.17813C>A	XP_016865452.1:p.Ala5938Asp
XM_017009964.2:c.17810C>A	XP_016865453.1:p.Ala5937Asp
XM_017009965.1:c.17810C>A	XP_016865454.1:p.Ala5937Asp
XM_017009966.2:c.17732C>A	XP_016865455.1:p.Ala5911Asp
XM_017009967.1:c.17717C>A	XP_016865456.1:p.Ala5906Asp
XM_017009968.2:c.17633C>A	XP_016865457.1:p.Ala5878Asp
XM_017009969.2:c.17813C>A	XP_016865458.1:p.Ala5938Asp
XM_017009972.1:c.10931C>A	XP_016865461.1:p.Ala3644Asp
XM_017009973.1:c.10910C>A	XP_016865462.1:p.Ala3637Asp