Canonical Allele Identifier: CA360431984
Community Standard Title: NM_032119.4(ADGRV1):c.18433-1G>A
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.91150029G>A , CM000667.2:g.91150029G>A GRCh38
NC_000005.9:g.90445846G>A , CM000667.1:g.90445846G>A GRCh37
NC_000005.8:g.90481602G>A NCBI36
NG_007083.1:g.596230G>A
NG_007083.2:g.625686G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.18433-1G>A MANE Select NP_115495.3:n.18433-1G>A
ENST00000405460.9:c.18433-1G>A MANE Select ENSP00000384582.2:n.18433-1G>A
NM_032119.3:c.18433-1G>A NP_115495.3:n.18433-1G>A
NR_003149.1:n.18446-1G>A
NR_003149.2:n.18449-1G>A
ENST00000405460.6:c.18433-1G>A ENSP00000384582.2:n.18433-1G>A
ENST00000425867.2:c.5416-1G>A ENSP00000392618.2:n.5416-1G>A
ENST00000425867.3:c.7387-1G>A ENSP00000392618.3:n.7387-1G>A
ENST00000638510.1:n.5700-1G>A
ENST00000638990.1:c.1645-1G>A
ENST00000639212.1:n.353-1G>A
ENST00000639530.1:n.301-1G>A
ENST00000639821.1:c.517-13753G>A ENSP00000492216.1:n.517-13753G>A
ENST00000640256.1:n.301-3192G>A
ENST00000640407.1:c.4882-1G>A ENSP00000491425.1:n.4882-1G>A
ENST00000640815.1:c.517-1G>A ENSP00000491767.1:n.517-1G>A
XM_011543675.1:c.18430-1G>A XP_011541977.1:n.18430-1G>A
XM_011543676.1:c.18352-1G>A XP_011541978.1:n.18352-1G>A
XM_011543677.1:c.15736-1G>A XP_011541979.1:n.15736-1G>A
XM_017009963.2:c.18454-1G>A XP_016865452.1:n.18454-1G>A
XM_017009964.2:c.18451-1G>A XP_016865453.1:n.18451-1G>A
XM_017009965.1:c.18451-1G>A XP_016865454.1:n.18451-1G>A
XM_017009966.2:c.18373-1G>A XP_016865455.1:n.18373-1G>A
XM_017009967.1:c.18358-1G>A XP_016865456.1:n.18358-1G>A
XM_017009968.2:c.18274-1G>A XP_016865457.1:n.18274-1G>A
XM_017009969.2:c.18454-13753G>A XP_016865458.1:n.18454-13753G>A
XM_017009972.1:c.11572-1G>A XP_016865461.1:n.11572-1G>A
XM_017009973.1:c.11551-1G>A XP_016865462.1:n.11551-1G>A
XR_001742796.1:n.225-14035C>T