Canonical Allele Identifier: CA3338513

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90625171A>G , CM000667.2:g.90625171A>G	GRCh38
NC_000005.9:g.89920988A>G , CM000667.1:g.89920988A>G	GRCh37
NC_000005.8:g.89956744A>G	NCBI36
NG_007083.1:g.71372A>G
NG_007083.2:g.100828A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.600A>G MANE Select	NP_115495.3:p.Pro200=
ENST00000405460.9:c.600A>G MANE Select	ENSP00000384582.2:p.Pro200=
NM_032119.3:c.600A>G	NP_115495.3:p.Pro200=
NR_003149.1:n.696A>G
NR_003149.2:n.699A>G
ENST00000405460.6:c.600A>G	ENSP00000384582.2:p.Pro200=
ENST00000638316.1:n.810A>G
ENST00000638638.1:n.1007A>G
ENST00000640083.1:n.305A>G
ENST00000640109.1:n.696A>G
ENST00000640281.1:n.659A>G
XM_011543675.1:c.600A>G	XP_011541977.1:p.Pro200=
XM_011543676.1:c.600A>G	XP_011541978.1:p.Pro200=
XM_011543678.1:c.600A>G	XP_011541980.1:p.Pro200=
XM_011543679.1:c.600A>G	XP_011541981.1:p.Pro200=
XM_017009963.2:c.600A>G	XP_016865452.1:p.Pro200=
XM_017009964.2:c.600A>G	XP_016865453.1:p.Pro200=
XM_017009965.1:c.597A>G	XP_016865454.1:p.Pro199=
XM_017009966.2:c.600A>G	XP_016865455.1:p.Pro200=
XM_017009967.1:c.504A>G	XP_016865456.1:p.Pro168=
XM_017009968.2:c.600A>G	XP_016865457.1:p.Pro200=
XM_017009969.2:c.600A>G	XP_016865458.1:p.Pro200=
XM_017009970.2:c.600A>G	XP_016865459.1:p.Pro200=
XM_017009971.2:c.600A>G	XP_016865460.1:p.Pro200=
XM_017009974.2:c.600A>G	XP_016865463.1:p.Pro200=