Canonical Allele Identifier: CA445415116

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728869A>G , CM000667.2:g.90728869A>G	GRCh38
NC_000005.9:g.90024686A>G , CM000667.1:g.90024686A>G	GRCh37
NC_000005.8:g.90060442A>G	NCBI36
NG_007083.1:g.175070A>G
NG_007083.2:g.204526A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10362A>G MANE Select	NP_115495.3:p.Thr3454=
ENST00000405460.9:c.10362A>G MANE Select	ENSP00000384582.2:p.Thr3454=
NM_032119.3:c.10362A>G	NP_115495.3:p.Thr3454=
NR_003149.1:n.10375A>G
NR_003149.2:n.10378A>G
ENST00000405460.6:c.10362A>G	ENSP00000384582.2:p.Thr3454=
ENST00000509621.1:c.3059A>G
ENST00000639431.1:c.265+52660A>G	ENSP00000491057.1:n.265+52660A>G
ENST00000640374.1:n.3506A>G
ENST00000640464.1:n.781A>G
XM_011543675.1:c.10359A>G	XP_011541977.1:p.Thr3453=
XM_011543676.1:c.10281A>G	XP_011541978.1:p.Thr3427=
XM_011543677.1:c.7665A>G	XP_011541979.1:p.Thr2555=
XM_011543678.1:c.10362A>G	XP_011541980.1:p.Thr3454=
XM_011543679.1:c.10362A>G	XP_011541981.1:p.Thr3454=
XM_017009963.2:c.10383A>G	XP_016865452.1:p.Thr3461=
XM_017009964.2:c.10380A>G	XP_016865453.1:p.Thr3460=
XM_017009965.1:c.10380A>G	XP_016865454.1:p.Thr3460=
XM_017009966.2:c.10302A>G	XP_016865455.1:p.Thr3434=
XM_017009967.1:c.10287A>G	XP_016865456.1:p.Thr3429=
XM_017009968.2:c.10383A>G	XP_016865457.1:p.Thr3461=
XM_017009969.2:c.10383A>G	XP_016865458.1:p.Thr3461=
XM_017009970.2:c.10383A>G	XP_016865459.1:p.Thr3461=
XM_017009971.2:c.10383A>G	XP_016865460.1:p.Thr3461=
XM_017009972.1:c.3501A>G	XP_016865461.1:p.Thr1167=
XM_017009973.1:c.3480A>G	XP_016865462.1:p.Thr1160=
XM_017009974.2:c.10383A>G	XP_016865463.1:p.Thr3461=
XR_001742802.1:n.2522+12038T>C
XR_948560.1:n.271+12038T>C