Canonical Allele Identifier: CA3340270
Community Standard Title: NM_032119.4(ADGRV1):c.8469T>G (p.His2823Gln)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90705482T>G , CM000667.2:g.90705482T>G GRCh38
NC_000005.9:g.90001299T>G , CM000667.1:g.90001299T>G GRCh37
NC_000005.8:g.90037055T>G NCBI36
NG_007083.1:g.151683T>G
NG_007083.2:g.181139T>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.8469T>G MANE Select NP_115495.3:p.His2823Gln
ENST00000405460.9:c.8469T>G MANE Select ENSP00000384582.2:p.His2823Gln
NM_032119.3:c.8469T>G NP_115495.3:p.His2823Gln
NR_003149.1:n.8482T>G
NR_003149.2:n.8485T>G
ENST00000405460.6:c.8469T>G ENSP00000384582.2:p.His2823Gln
ENST00000509621.1:c.1166T>G
ENST00000639431.1:c.265+29273T>G ENSP00000491057.1:n.265+29273T>G
ENST00000639473.1:n.3928T>G
ENST00000640012.1:c.2276T>G
ENST00000640374.1:n.1613T>G
ENST00000640403.1:c.5760T>G ENSP00000492531.1:p.His1920Gln
ENST00000640779.1:c.3198T>G
XM_011543675.1:c.8466T>G XP_011541977.1:p.His2822Gln
XM_011543676.1:c.8388T>G XP_011541978.1:p.His2796Gln
XM_011543677.1:c.5772T>G XP_011541979.1:p.His1924Gln
XM_011543678.1:c.8469T>G XP_011541980.1:p.His2823Gln
XM_011543679.1:c.8469T>G XP_011541981.1:p.His2823Gln
XM_017009963.2:c.8490T>G XP_016865452.1:p.His2830Gln
XM_017009964.2:c.8487T>G XP_016865453.1:p.His2829Gln
XM_017009965.1:c.8487T>G XP_016865454.1:p.His2829Gln
XM_017009966.2:c.8409T>G XP_016865455.1:p.His2803Gln
XM_017009967.1:c.8394T>G XP_016865456.1:p.His2798Gln
XM_017009968.2:c.8490T>G XP_016865457.1:p.His2830Gln
XM_017009969.2:c.8490T>G XP_016865458.1:p.His2830Gln
XM_017009970.2:c.8490T>G XP_016865459.1:p.His2830Gln
XM_017009971.2:c.8490T>G XP_016865460.1:p.His2830Gln
XM_017009972.1:c.1608T>G XP_016865461.1:p.His536Gln
XM_017009973.1:c.1587T>G XP_016865462.1:p.His529Gln
XM_017009974.2:c.8490T>G XP_016865463.1:p.His2830Gln