Canonical Allele Identifier: CA3341977

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90811029A>G , CM000667.2:g.90811029A>G	GRCh38
NC_000005.9:g.90106846A>G , CM000667.1:g.90106846A>G	GRCh37
NC_000005.8:g.90142602A>G	NCBI36
NG_007083.1:g.257230A>G
NG_007083.2:g.286686A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15769A>G MANE Select	NP_115495.3:p.Ile5257Val
ENST00000405460.9:c.15769A>G MANE Select	ENSP00000384582.2:p.Ile5257Val
NM_032119.3:c.15769A>G	NP_115495.3:p.Ile5257Val
NR_003149.1:n.15782A>G
NR_003149.2:n.15785A>G
ENST00000405460.6:c.15769A>G	ENSP00000384582.2:p.Ile5257Val
ENST00000425867.2:c.2752A>G	ENSP00000392618.2:p.Ile918Val
ENST00000425867.3:c.4723A>G	ENSP00000392618.3:p.Ile1575Val
ENST00000638510.1:n.3036A>G
ENST00000639431.1:c.265+134820A>G	ENSP00000491057.1:n.265+134820A>G
ENST00000640407.1:c.2179A>G	ENSP00000491425.1:p.Ile727Val
XM_011543675.1:c.15766A>G	XP_011541977.1:p.Ile5256Val
XM_011543676.1:c.15688A>G	XP_011541978.1:p.Ile5230Val
XM_011543677.1:c.13072A>G	XP_011541979.1:p.Ile4358Val
XM_017009963.2:c.15790A>G	XP_016865452.1:p.Ile5264Val
XM_017009964.2:c.15787A>G	XP_016865453.1:p.Ile5263Val
XM_017009965.1:c.15787A>G	XP_016865454.1:p.Ile5263Val
XM_017009966.2:c.15709A>G	XP_016865455.1:p.Ile5237Val
XM_017009967.1:c.15694A>G	XP_016865456.1:p.Ile5232Val
XM_017009968.2:c.15610A>G	XP_016865457.1:p.Ile5204Val
XM_017009969.2:c.15790A>G	XP_016865458.1:p.Ile5264Val
XM_017009972.1:c.8908A>G	XP_016865461.1:p.Ile2970Val
XM_017009973.1:c.8887A>G	XP_016865462.1:p.Ile2963Val