Canonical Allele Identifier: CA3339757

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90685831T>C , CM000667.2:g.90685831T>C	GRCh38
NC_000005.9:g.89981648T>C , CM000667.1:g.89981648T>C	GRCh37
NC_000005.8:g.90017404T>C	NCBI36
NG_007083.1:g.132032T>C
NG_007083.2:g.161488T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.6326T>C MANE Select	NP_115495.3:p.Ile2109Thr
ENST00000405460.9:c.6326T>C MANE Select	ENSP00000384582.2:p.Ile2109Thr
NM_032119.3:c.6326T>C	NP_115495.3:p.Ile2109Thr
NR_003149.1:n.6422T>C
NR_003149.2:n.6425T>C
ENST00000405460.6:c.6326T>C	ENSP00000384582.2:p.Ile2109Thr
ENST00000639431.1:c.265+9622T>C	ENSP00000491057.1:n.265+9622T>C
ENST00000639473.1:n.1785T>C
ENST00000640012.1:c.216T>C
ENST00000640403.1:c.3617T>C	ENSP00000492531.1:p.Ile1206Thr
ENST00000640779.1:c.1138T>C
XM_011543675.1:c.6323T>C	XP_011541977.1:p.Ile2108Thr
XM_011543676.1:c.6245T>C	XP_011541978.1:p.Ile2082Thr
XM_011543677.1:c.3629T>C	XP_011541979.1:p.Ile1210Thr
XM_011543678.1:c.6326T>C	XP_011541980.1:p.Ile2109Thr
XM_011543679.1:c.6326T>C	XP_011541981.1:p.Ile2109Thr
XM_017009963.2:c.6326T>C	XP_016865452.1:p.Ile2109Thr
XM_017009964.2:c.6323T>C	XP_016865453.1:p.Ile2108Thr
XM_017009965.1:c.6323T>C	XP_016865454.1:p.Ile2108Thr
XM_017009966.2:c.6245T>C	XP_016865455.1:p.Ile2082Thr
XM_017009967.1:c.6230T>C	XP_016865456.1:p.Ile2077Thr
XM_017009968.2:c.6326T>C	XP_016865457.1:p.Ile2109Thr
XM_017009969.2:c.6326T>C	XP_016865458.1:p.Ile2109Thr
XM_017009970.2:c.6326T>C	XP_016865459.1:p.Ile2109Thr
XM_017009971.2:c.6326T>C	XP_016865460.1:p.Ile2109Thr
XM_017009973.1:c.-474T>C	XP_016865462.1:n.-474T>C
XM_017009974.2:c.6326T>C	XP_016865463.1:p.Ile2109Thr