Canonical Allele Identifier: CA561261561

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91150017T>C , CM000667.2:g.91150017T>C	GRCh38
NC_000005.9:g.90445834T>C , CM000667.1:g.90445834T>C	GRCh37
NC_000005.8:g.90481590T>C	NCBI36
NG_007083.1:g.596218T>C
NG_007083.2:g.625674T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18433-13T>C MANE Select	NP_115495.3:n.18433-13T>C
ENST00000405460.9:c.18433-13T>C MANE Select	ENSP00000384582.2:n.18433-13T>C
NM_032119.3:c.18433-13T>C	NP_115495.3:n.18433-13T>C
NR_003149.1:n.18446-13T>C
NR_003149.2:n.18449-13T>C
ENST00000405460.6:c.18433-13T>C	ENSP00000384582.2:n.18433-13T>C
ENST00000425867.2:c.5416-13T>C	ENSP00000392618.2:n.5416-13T>C
ENST00000425867.3:c.7387-13T>C	ENSP00000392618.3:n.7387-13T>C
ENST00000638510.1:n.5700-13T>C
ENST00000638990.1:c.1645-13T>C
ENST00000639212.1:n.353-13T>C
ENST00000639530.1:n.301-13T>C
ENST00000639821.1:c.517-13765T>C	ENSP00000492216.1:n.517-13765T>C
ENST00000640256.1:n.301-3204T>C
ENST00000640407.1:c.4882-13T>C	ENSP00000491425.1:n.4882-13T>C
ENST00000640815.1:c.517-13T>C	ENSP00000491767.1:n.517-13T>C
XM_011543675.1:c.18430-13T>C	XP_011541977.1:n.18430-13T>C
XM_011543676.1:c.18352-13T>C	XP_011541978.1:n.18352-13T>C
XM_011543677.1:c.15736-13T>C	XP_011541979.1:n.15736-13T>C
XM_017009963.2:c.18454-13T>C	XP_016865452.1:n.18454-13T>C
XM_017009964.2:c.18451-13T>C	XP_016865453.1:n.18451-13T>C
XM_017009965.1:c.18451-13T>C	XP_016865454.1:n.18451-13T>C
XM_017009966.2:c.18373-13T>C	XP_016865455.1:n.18373-13T>C
XM_017009967.1:c.18358-13T>C	XP_016865456.1:n.18358-13T>C
XM_017009968.2:c.18274-13T>C	XP_016865457.1:n.18274-13T>C
XM_017009969.2:c.18454-13765T>C	XP_016865458.1:n.18454-13765T>C
XM_017009972.1:c.11572-13T>C	XP_016865461.1:n.11572-13T>C
XM_017009973.1:c.11551-13T>C	XP_016865462.1:n.11551-13T>C
XR_001742796.1:n.225-14023A>G