Canonical Allele Identifier: CA360367199
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755150A>T , CM000667.2:g.90755150A>T GRCh38
NC_000005.9:g.90050967A>T , CM000667.1:g.90050967A>T GRCh37
NC_000005.8:g.90086723A>T NCBI36
NG_007083.1:g.201351A>T
NG_007083.2:g.230807A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11545A>T MANE Select ENSP00000384582.2:p.Ile3849Leu
ENST00000425867.3:c.676A>T ENSP00000392618.3:p.Ile226Leu
ENST00000639431.1:c.265+78941A>T ENSP00000491057.1:n.265+78941A>T
ENST00000640374.1:n.4689A>T
ENST00000640464.1:n.1964A>T
ENST00000405460.6:c.11545A>T ENSP00000384582.2:p.Ile3849Leu
ENST00000509621.1:c.4242A>T
NM_032119.3:c.11545A>T NP_115495.3:p.Ile3849Leu
NR_003149.1:n.11558A>T
XM_011543675.1:c.11542A>T XP_011541977.1:p.Ile3848Leu
XM_011543676.1:c.11464A>T XP_011541978.1:p.Ile3822Leu
XM_011543677.1:c.8848A>T XP_011541979.1:p.Ile2950Leu
XM_011543678.1:c.11545A>T XP_011541980.1:p.Ile3849Leu
NM_032119.4:c.11545A>T MANE Select NP_115495.3:p.Ile3849Leu
XM_017009963.2:c.11566A>T XP_016865452.1:p.Ile3856Leu
XM_017009964.2:c.11563A>T XP_016865453.1:p.Ile3855Leu
XM_017009965.1:c.11563A>T XP_016865454.1:p.Ile3855Leu
XM_017009966.2:c.11485A>T XP_016865455.1:p.Ile3829Leu
XM_017009967.1:c.11470A>T XP_016865456.1:p.Ile3824Leu
XM_017009968.2:c.11566A>T XP_016865457.1:p.Ile3856Leu
XM_017009969.2:c.11566A>T XP_016865458.1:p.Ile3856Leu
XM_017009970.2:c.11566A>T XP_016865459.1:p.Ile3856Leu
XM_017009971.2:c.11566A>T XP_016865460.1:p.Ile3856Leu
XM_017009972.1:c.4684A>T XP_016865461.1:p.Ile1562Leu
XM_017009973.1:c.4663A>T XP_016865462.1:p.Ile1555Leu
NR_003149.2:n.11561A>T