Canonical Allele Identifier: CA122821802

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810765A>G , CM000667.2:g.90810765A>G	GRCh38
NC_000005.9:g.90106582A>G , CM000667.1:g.90106582A>G	GRCh37
NC_000005.8:g.90142338A>G	NCBI36
NG_007083.1:g.256966A>G
NG_007083.2:g.286422A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15505A>G MANE Select	NP_115495.3:p.Ile5169Val
ENST00000405460.9:c.15505A>G MANE Select	ENSP00000384582.2:p.Ile5169Val
NM_032119.3:c.15505A>G	NP_115495.3:p.Ile5169Val
NR_003149.1:n.15518A>G
NR_003149.2:n.15521A>G
ENST00000405460.6:c.15505A>G	ENSP00000384582.2:p.Ile5169Val
ENST00000425867.2:c.2488A>G	ENSP00000392618.2:p.Ile830Val
ENST00000425867.3:c.4459A>G	ENSP00000392618.3:p.Ile1487Val
ENST00000638510.1:n.2772A>G
ENST00000639431.1:c.265+134556A>G	ENSP00000491057.1:n.265+134556A>G
ENST00000640407.1:c.1915A>G	ENSP00000491425.1:p.Ile639Val
XM_011543675.1:c.15502A>G	XP_011541977.1:p.Ile5168Val
XM_011543676.1:c.15424A>G	XP_011541978.1:p.Ile5142Val
XM_011543677.1:c.12808A>G	XP_011541979.1:p.Ile4270Val
XM_017009963.2:c.15526A>G	XP_016865452.1:p.Ile5176Val
XM_017009964.2:c.15523A>G	XP_016865453.1:p.Ile5175Val
XM_017009965.1:c.15523A>G	XP_016865454.1:p.Ile5175Val
XM_017009966.2:c.15445A>G	XP_016865455.1:p.Ile5149Val
XM_017009967.1:c.15430A>G	XP_016865456.1:p.Ile5144Val
XM_017009968.2:c.15346A>G	XP_016865457.1:p.Ile5116Val
XM_017009969.2:c.15526A>G	XP_016865458.1:p.Ile5176Val
XM_017009971.2:c.*459A>G	XP_016865460.1:n.*459A>G
XM_017009972.1:c.8644A>G	XP_016865461.1:p.Ile2882Val
XM_017009973.1:c.8623A>G	XP_016865462.1:p.Ile2875Val