Canonical Allele Identifier: CA3340673
Community Standard Title: NM_032119.4(ADGRV1):c.10142A>G (p.Asp3381Gly)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90725637A>G , CM000667.2:g.90725637A>G GRCh38
NC_000005.9:g.90021454A>G , CM000667.1:g.90021454A>G GRCh37
NC_000005.8:g.90057210A>G NCBI36
NG_007083.1:g.171838A>G
NG_007083.2:g.201294A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.10142A>G MANE Select NP_115495.3:p.Asp3381Gly
ENST00000405460.9:c.10142A>G MANE Select ENSP00000384582.2:p.Asp3381Gly
NM_032119.3:c.10142A>G NP_115495.3:p.Asp3381Gly
NR_003149.1:n.10155A>G
NR_003149.2:n.10158A>G
ENST00000405460.6:c.10142A>G ENSP00000384582.2:p.Asp3381Gly
ENST00000509621.1:c.2839A>G
ENST00000639431.1:c.265+49428A>G ENSP00000491057.1:n.265+49428A>G
ENST00000640374.1:n.3286A>G
ENST00000640464.1:n.561A>G
XM_011543675.1:c.10139A>G XP_011541977.1:p.Asp3380Gly
XM_011543676.1:c.10061A>G XP_011541978.1:p.Asp3354Gly
XM_011543677.1:c.7445A>G XP_011541979.1:p.Asp2482Gly
XM_011543678.1:c.10142A>G XP_011541980.1:p.Asp3381Gly
XM_011543679.1:c.10142A>G XP_011541981.1:p.Asp3381Gly
XM_017009963.2:c.10163A>G XP_016865452.1:p.Asp3388Gly
XM_017009964.2:c.10160A>G XP_016865453.1:p.Asp3387Gly
XM_017009965.1:c.10160A>G XP_016865454.1:p.Asp3387Gly
XM_017009966.2:c.10082A>G XP_016865455.1:p.Asp3361Gly
XM_017009967.1:c.10067A>G XP_016865456.1:p.Asp3356Gly
XM_017009968.2:c.10163A>G XP_016865457.1:p.Asp3388Gly
XM_017009969.2:c.10163A>G XP_016865458.1:p.Asp3388Gly
XM_017009970.2:c.10163A>G XP_016865459.1:p.Asp3388Gly
XM_017009971.2:c.10163A>G XP_016865460.1:p.Asp3388Gly
XM_017009972.1:c.3281A>G XP_016865461.1:p.Asp1094Gly
XM_017009973.1:c.3260A>G XP_016865462.1:p.Asp1087Gly
XM_017009974.2:c.10163A>G XP_016865463.1:p.Asp3388Gly
XR_001742802.1:n.2523-9828T>C
XR_948560.1:n.272-9828T>C