Canonical Allele Identifier: CA3342264

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90840965A>G , CM000667.2:g.90840965A>G	GRCh38
NC_000005.9:g.90136782A>G , CM000667.1:g.90136782A>G	GRCh37
NC_000005.8:g.90172538A>G	NCBI36
NG_007083.1:g.287166A>G
NG_007083.2:g.316622A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16999A>G MANE Select	NP_115495.3:p.Met5667Val
ENST00000405460.9:c.16999A>G MANE Select	ENSP00000384582.2:p.Met5667Val
NM_032119.3:c.16999A>G	NP_115495.3:p.Met5667Val
NR_003149.1:n.17012A>G
NR_003149.2:n.17015A>G
ENST00000405460.6:c.16999A>G	ENSP00000384582.2:p.Met5667Val
ENST00000425867.2:c.3982A>G	ENSP00000392618.2:p.Met1328Val
ENST00000425867.3:c.5953A>G	ENSP00000392618.3:p.Met1985Val
ENST00000638510.1:n.4266A>G
ENST00000638990.1:c.20A>G
ENST00000639431.1:c.266-144379A>G	ENSP00000491057.1:n.266-144379A>G
ENST00000640061.1:n.516A>G
ENST00000640407.1:c.3448A>G	ENSP00000491425.1:n.3448A>G
XM_011543675.1:c.16996A>G	XP_011541977.1:p.Met5666Val
XM_011543676.1:c.16918A>G	XP_011541978.1:p.Met5640Val
XM_011543677.1:c.14302A>G	XP_011541979.1:p.Met4768Val
XM_017009963.2:c.17020A>G	XP_016865452.1:p.Met5674Val
XM_017009964.2:c.17017A>G	XP_016865453.1:p.Met5673Val
XM_017009965.1:c.17017A>G	XP_016865454.1:p.Met5673Val
XM_017009966.2:c.16939A>G	XP_016865455.1:p.Met5647Val
XM_017009967.1:c.16924A>G	XP_016865456.1:p.Met5642Val
XM_017009968.2:c.16840A>G	XP_016865457.1:p.Met5614Val
XM_017009969.2:c.17020A>G	XP_016865458.1:p.Met5674Val
XM_017009972.1:c.10138A>G	XP_016865461.1:p.Met3380Val
XM_017009973.1:c.10117A>G	XP_016865462.1:p.Met3373Val