Canonical Allele Identifier: CA3342248

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90840878C>A , CM000667.2:g.90840878C>A	GRCh38
NC_000005.9:g.90136695C>A , CM000667.1:g.90136695C>A	GRCh37
NC_000005.8:g.90172451C>A	NCBI36
NG_007083.1:g.287079C>A
NG_007083.2:g.316535C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16912C>A MANE Select	NP_115495.3:p.Pro5638Thr
ENST00000405460.9:c.16912C>A MANE Select	ENSP00000384582.2:p.Pro5638Thr
NM_032119.3:c.16912C>A	NP_115495.3:p.Pro5638Thr
NR_003149.1:n.16925C>A
NR_003149.2:n.16928C>A
ENST00000405460.6:c.16912C>A	ENSP00000384582.2:p.Pro5638Thr
ENST00000425867.2:c.3895C>A	ENSP00000392618.2:p.Pro1299Thr
ENST00000425867.3:c.5866C>A	ENSP00000392618.3:p.Pro1956Thr
ENST00000638510.1:n.4179C>A
ENST00000639431.1:c.266-144466C>A	ENSP00000491057.1:n.266-144466C>A
ENST00000640061.1:n.429C>A
ENST00000640407.1:c.3361C>A	ENSP00000491425.1:n.3361C>A
XM_011543675.1:c.16909C>A	XP_011541977.1:p.Pro5637Thr
XM_011543676.1:c.16831C>A	XP_011541978.1:p.Pro5611Thr
XM_011543677.1:c.14215C>A	XP_011541979.1:p.Pro4739Thr
XM_017009963.2:c.16933C>A	XP_016865452.1:p.Pro5645Thr
XM_017009964.2:c.16930C>A	XP_016865453.1:p.Pro5644Thr
XM_017009965.1:c.16930C>A	XP_016865454.1:p.Pro5644Thr
XM_017009966.2:c.16852C>A	XP_016865455.1:p.Pro5618Thr
XM_017009967.1:c.16837C>A	XP_016865456.1:p.Pro5613Thr
XM_017009968.2:c.16753C>A	XP_016865457.1:p.Pro5585Thr
XM_017009969.2:c.16933C>A	XP_016865458.1:p.Pro5645Thr
XM_017009972.1:c.10051C>A	XP_016865461.1:p.Pro3351Thr
XM_017009973.1:c.10030C>A	XP_016865462.1:p.Pro3344Thr