Canonical Allele Identifier: CA3342800

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91164159A>G , CM000667.2:g.91164159A>G	GRCh38
NC_000005.9:g.90459976A>G , CM000667.1:g.90459976A>G	GRCh37
NC_000005.8:g.90495732A>G	NCBI36
NG_007083.1:g.610360A>G
NG_007083.2:g.639816A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.*259A>G MANE Select	NP_115495.3:n.*259A>G
ENST00000405460.9:c.*259A>G MANE Select	ENSP00000384582.2:n.*259A>G
NM_032119.3:c.*259A>G	NP_115495.3:n.*259A>G
NR_003149.1:n.19193A>G
NR_003149.2:n.19196A>G
ENST00000405460.6:c.*259A>G	ENSP00000384582.2:n.*259A>G
ENST00000425867.2:c.*259A>G	ENSP00000392618.2:n.*259A>G
ENST00000425867.3:c.8134A>G	ENSP00000392618.3:n.8134A>G
ENST00000638510.1:n.6447A>G
ENST00000638990.1:c.2392A>G
ENST00000639212.1:n.1100A>G
ENST00000639530.1:n.1048A>G
ENST00000640256.1:n.856A>G
ENST00000640407.1:c.5629A>G	ENSP00000491425.1:n.5629A>G
ENST00000640815.1:c.*259A>G	ENSP00000491767.1:n.*259A>G
XM_011543675.1:c.*259A>G	XP_011541977.1:n.*259A>G
XM_011543676.1:c.*259A>G	XP_011541978.1:n.*259A>G
XM_011543677.1:c.*259A>G	XP_011541979.1:n.*259A>G
XM_017009963.2:c.*259A>G	XP_016865452.1:n.*259A>G
XM_017009964.2:c.*259A>G	XP_016865453.1:n.*259A>G
XM_017009965.1:c.*259A>G	XP_016865454.1:n.*259A>G
XM_017009966.2:c.*259A>G	XP_016865455.1:n.*259A>G
XM_017009967.1:c.*259A>G	XP_016865456.1:n.*259A>G
XM_017009968.2:c.*259A>G	XP_016865457.1:n.*259A>G
XM_017009969.2:c.*315A>G	XP_016865458.1:n.*315A>G
XM_017009972.1:c.*259A>G	XP_016865461.1:n.*259A>G
XM_017009973.1:c.*259A>G	XP_016865462.1:n.*259A>G
XR_001742795.1:n.225-11971T>C
XR_001742796.1:n.225-28165T>C
XR_001742797.1:n.225-2855T>C