Canonical Allele Identifier: CA360403203
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90725568T>G , CM000667.2:g.90725568T>G GRCh38
NC_000005.9:g.90021385T>G , CM000667.1:g.90021385T>G GRCh37
NC_000005.8:g.90057141T>G NCBI36
NG_007083.1:g.171769T>G
NG_007083.2:g.201225T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.10073T>G MANE Select ENSP00000384582.2:p.Leu3358Arg
ENST00000639431.1:c.265+49359T>G ENSP00000491057.1:n.265+49359T>G
ENST00000640374.1:n.3217T>G
ENST00000640464.1:n.492T>G
ENST00000405460.6:c.10073T>G ENSP00000384582.2:p.Leu3358Arg
ENST00000509621.1:c.2770T>G
NM_032119.3:c.10073T>G NP_115495.3:p.Leu3358Arg
NR_003149.1:n.10086T>G
XM_011543675.1:c.10070T>G XP_011541977.1:p.Leu3357Arg
XM_011543676.1:c.9992T>G XP_011541978.1:p.Leu3331Arg
XM_011543677.1:c.7376T>G XP_011541979.1:p.Leu2459Arg
XM_011543678.1:c.10073T>G XP_011541980.1:p.Leu3358Arg
XM_011543679.1:c.10073T>G XP_011541981.1:p.Leu3358Arg
XR_948560.1:n.272-9759A>C
NM_032119.4:c.10073T>G MANE Select NP_115495.3:p.Leu3358Arg
XM_017009963.2:c.10094T>G XP_016865452.1:p.Leu3365Arg
XM_017009964.2:c.10091T>G XP_016865453.1:p.Leu3364Arg
XM_017009965.1:c.10091T>G XP_016865454.1:p.Leu3364Arg
XM_017009966.2:c.10013T>G XP_016865455.1:p.Leu3338Arg
XM_017009967.1:c.9998T>G XP_016865456.1:p.Leu3333Arg
XM_017009968.2:c.10094T>G XP_016865457.1:p.Leu3365Arg
XM_017009969.2:c.10094T>G XP_016865458.1:p.Leu3365Arg
XM_017009970.2:c.10094T>G XP_016865459.1:p.Leu3365Arg
XM_017009971.2:c.10094T>G XP_016865460.1:p.Leu3365Arg
XM_017009972.1:c.3212T>G XP_016865461.1:p.Leu1071Arg
XM_017009973.1:c.3191T>G XP_016865462.1:p.Leu1064Arg
XM_017009974.2:c.10094T>G XP_016865463.1:p.Leu3365Arg
XR_001742802.1:n.2523-9759A>C
NR_003149.2:n.10089T>G