Canonical Allele Identifier: CA360399423
Community Standard Title: NM_032119.4(ADGRV1):c.9479A>T (p.Glu3160Val)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90720079A>T , CM000667.2:g.90720079A>T GRCh38
NC_000005.9:g.90015896A>T , CM000667.1:g.90015896A>T GRCh37
NC_000005.8:g.90051652A>T NCBI36
NG_007083.1:g.166280A>T
NG_007083.2:g.195736A>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.9479A>T MANE Select NP_115495.3:p.Glu3160Val
ENST00000405460.9:c.9479A>T MANE Select ENSP00000384582.2:p.Glu3160Val
NM_032119.3:c.9479A>T NP_115495.3:p.Glu3160Val
NR_003149.1:n.9492A>T
NR_003149.2:n.9495A>T
ENST00000405460.6:c.9479A>T ENSP00000384582.2:p.Glu3160Val
ENST00000509621.1:c.2176A>T
ENST00000639431.1:c.265+43870A>T ENSP00000491057.1:n.265+43870A>T
ENST00000640374.1:n.2623A>T
ENST00000640779.1:c.4208A>T
XM_011543675.1:c.9476A>T XP_011541977.1:p.Glu3159Val
XM_011543676.1:c.9398A>T XP_011541978.1:p.Glu3133Val
XM_011543677.1:c.6782A>T XP_011541979.1:p.Glu2261Val
XM_011543678.1:c.9479A>T XP_011541980.1:p.Glu3160Val
XM_011543679.1:c.9479A>T XP_011541981.1:p.Glu3160Val
XM_017009963.2:c.9500A>T XP_016865452.1:p.Glu3167Val
XM_017009964.2:c.9497A>T XP_016865453.1:p.Glu3166Val
XM_017009965.1:c.9497A>T XP_016865454.1:p.Glu3166Val
XM_017009966.2:c.9419A>T XP_016865455.1:p.Glu3140Val
XM_017009967.1:c.9404A>T XP_016865456.1:p.Glu3135Val
XM_017009968.2:c.9500A>T XP_016865457.1:p.Glu3167Val
XM_017009969.2:c.9500A>T XP_016865458.1:p.Glu3167Val
XM_017009970.2:c.9500A>T XP_016865459.1:p.Glu3167Val
XM_017009971.2:c.9500A>T XP_016865460.1:p.Glu3167Val
XM_017009972.1:c.2618A>T XP_016865461.1:p.Glu873Val
XM_017009973.1:c.2597A>T XP_016865462.1:p.Glu866Val
XM_017009974.2:c.9500A>T XP_016865463.1:p.Glu3167Val
XR_001742802.1:n.2523-4270T>A
XR_948560.1:n.272-4270T>A