Canonical Allele Identifier: CA360432428
Community Standard Title: NM_032119.4(ADGRV1):c.18625-2A>G
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.91153219A>G , CM000667.2:g.91153219A>G GRCh38
NC_000005.9:g.90449036A>G , CM000667.1:g.90449036A>G GRCh37
NC_000005.8:g.90484792A>G NCBI36
NG_007083.1:g.599420A>G
NG_007083.2:g.628876A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.18625-2A>G MANE Select NP_115495.3:n.18625-2A>G
ENST00000405460.9:c.18625-2A>G MANE Select ENSP00000384582.2:n.18625-2A>G
NM_032119.3:c.18625-2A>G NP_115495.3:n.18625-2A>G
NR_003149.1:n.18638-2A>G
NR_003149.2:n.18641-2A>G
ENST00000405460.6:c.18625-2A>G ENSP00000384582.2:n.18625-2A>G
ENST00000425867.2:c.5608-2A>G ENSP00000392618.2:n.5608-2A>G
ENST00000425867.3:c.7579-2A>G ENSP00000392618.3:n.7579-2A>G
ENST00000638510.1:n.5892-2A>G
ENST00000638990.1:c.1837-2A>G
ENST00000639212.1:n.545-2A>G
ENST00000639530.1:n.493-2A>G
ENST00000639821.1:c.517-10563A>G ENSP00000492216.1:n.517-10563A>G
ENST00000640256.1:n.301-2A>G
ENST00000640407.1:c.5074-2A>G ENSP00000491425.1:n.5074-2A>G
ENST00000640815.1:c.709-2A>G ENSP00000491767.1:n.709-2A>G
XM_011543675.1:c.18622-2A>G XP_011541977.1:n.18622-2A>G
XM_011543676.1:c.18544-2A>G XP_011541978.1:n.18544-2A>G
XM_011543677.1:c.15928-2A>G XP_011541979.1:n.15928-2A>G
XM_017009963.2:c.18646-2A>G XP_016865452.1:n.18646-2A>G
XM_017009964.2:c.18643-2A>G XP_016865453.1:n.18643-2A>G
XM_017009965.1:c.18643-2A>G XP_016865454.1:n.18643-2A>G
XM_017009966.2:c.18565-2A>G XP_016865455.1:n.18565-2A>G
XM_017009967.1:c.18550-2A>G XP_016865456.1:n.18550-2A>G
XM_017009968.2:c.18466-2A>G XP_016865457.1:n.18466-2A>G
XM_017009969.2:c.18454-10563A>G XP_016865458.1:n.18454-10563A>G
XM_017009972.1:c.11764-2A>G XP_016865461.1:n.11764-2A>G
XM_017009973.1:c.11743-2A>G XP_016865462.1:n.11743-2A>G
XR_001742795.1:n.225-1031T>C
XR_001742796.1:n.225-17225T>C