Canonical Allele Identifier: CA360389756
Community Standard Title: NM_032119.4(ADGRV1):c.8310T>A (p.Phe2770Leu)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90704412T>A , CM000667.2:g.90704412T>A GRCh38
NC_000005.9:g.90000229T>A , CM000667.1:g.90000229T>A GRCh37
NC_000005.8:g.90035985T>A NCBI36
NG_007083.1:g.150613T>A
NG_007083.2:g.180069T>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.8310T>A MANE Select NP_115495.3:p.Phe2770Leu
ENST00000405460.9:c.8310T>A MANE Select ENSP00000384582.2:p.Phe2770Leu
NM_032119.3:c.8310T>A NP_115495.3:p.Phe2770Leu
NR_003149.1:n.8323T>A
NR_003149.2:n.8326T>A
ENST00000405460.6:c.8310T>A ENSP00000384582.2:p.Phe2770Leu
ENST00000509621.1:c.1007T>A
ENST00000639431.1:c.265+28203T>A ENSP00000491057.1:n.265+28203T>A
ENST00000639473.1:n.3769T>A
ENST00000640012.1:c.2117T>A
ENST00000640374.1:n.1454T>A
ENST00000640403.1:c.5601T>A ENSP00000492531.1:p.Phe1867Leu
ENST00000640779.1:c.3039T>A
XM_011543675.1:c.8307T>A XP_011541977.1:p.Phe2769Leu
XM_011543676.1:c.8229T>A XP_011541978.1:p.Phe2743Leu
XM_011543677.1:c.5613T>A XP_011541979.1:p.Phe1871Leu
XM_011543678.1:c.8310T>A XP_011541980.1:p.Phe2770Leu
XM_011543679.1:c.8310T>A XP_011541981.1:p.Phe2770Leu
XM_017009963.2:c.8310T>A XP_016865452.1:p.Phe2770Leu
XM_017009964.2:c.8307T>A XP_016865453.1:p.Phe2769Leu
XM_017009965.1:c.8307T>A XP_016865454.1:p.Phe2769Leu
XM_017009966.2:c.8229T>A XP_016865455.1:p.Phe2743Leu
XM_017009967.1:c.8214T>A XP_016865456.1:p.Phe2738Leu
XM_017009968.2:c.8310T>A XP_016865457.1:p.Phe2770Leu
XM_017009969.2:c.8310T>A XP_016865458.1:p.Phe2770Leu
XM_017009970.2:c.8310T>A XP_016865459.1:p.Phe2770Leu
XM_017009971.2:c.8310T>A XP_016865460.1:p.Phe2770Leu
XM_017009972.1:c.1428T>A XP_016865461.1:p.Phe476Leu
XM_017009973.1:c.1428T>A XP_016865462.1:p.Phe476Leu
XM_017009974.2:c.8310T>A XP_016865463.1:p.Phe2770Leu