Canonical Allele Identifier: CA360429091
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90985371A>C , CM000667.2:g.90985371A>C GRCh38
NC_000005.9:g.90281188A>C , CM000667.1:g.90281188A>C GRCh37
NC_000005.8:g.90316944A>C NCBI36
NG_007083.1:g.431572A>C
NG_007083.2:g.461028A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.18001A>C MANE Select ENSP00000384582.2:p.Met6001Leu
ENST00000425867.3:c.6955A>C ENSP00000392618.3:p.Met2319Leu
ENST00000638510.1:n.5268A>C
ENST00000638990.1:c.1213A>C
ENST00000639431.1:c.293A>C ENSP00000491057.1:p.Asp98Ala
ENST00000639707.1:c.85A>C ENSP00000492328.1:p.Met29Leu
ENST00000639821.1:c.85A>C ENSP00000492216.1:p.Met29Leu
ENST00000640369.1:c.85A>C ENSP00000491401.1:p.Met29Leu
ENST00000640407.1:c.4450A>C ENSP00000491425.1:n.4450A>C
ENST00000640815.1:c.85A>C ENSP00000491767.1:p.Met29Leu
ENST00000405460.6:c.18001A>C ENSP00000384582.2:p.Met6001Leu
ENST00000425867.2:c.4984A>C ENSP00000392618.2:p.Met1662Leu
NM_032119.3:c.18001A>C NP_115495.3:p.Met6001Leu
NR_003149.1:n.18014A>C
XM_011543675.1:c.17998A>C XP_011541977.1:p.Met6000Leu
XM_011543676.1:c.17920A>C XP_011541978.1:p.Met5974Leu
XM_011543677.1:c.15304A>C XP_011541979.1:p.Met5102Leu
NM_032119.4:c.18001A>C MANE Select NP_115495.3:p.Met6001Leu
XM_017009963.2:c.18022A>C XP_016865452.1:p.Met6008Leu
XM_017009964.2:c.18019A>C XP_016865453.1:p.Met6007Leu
XM_017009965.1:c.18019A>C XP_016865454.1:p.Met6007Leu
XM_017009966.2:c.17941A>C XP_016865455.1:p.Met5981Leu
XM_017009967.1:c.17926A>C XP_016865456.1:p.Met5976Leu
XM_017009968.2:c.17842A>C XP_016865457.1:p.Met5948Leu
XM_017009969.2:c.18022A>C XP_016865458.1:p.Met6008Leu
XM_017009972.1:c.11140A>C XP_016865461.1:p.Met3714Leu
XM_017009973.1:c.11119A>C XP_016865462.1:p.Met3707Leu
NR_003149.2:n.18017A>C