Canonical Allele Identifier: CA3341923
Community Standard Title: NM_032119.4(ADGRV1):c.15440A>G (p.Asp5147Gly)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90810700A>G , CM000667.2:g.90810700A>G GRCh38
NC_000005.9:g.90106517A>G , CM000667.1:g.90106517A>G GRCh37
NC_000005.8:g.90142273A>G NCBI36
NG_007083.1:g.256901A>G
NG_007083.2:g.286357A>G

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.15440A>G MANE Select NP_115495.3:p.Asp5147Gly
ENST00000405460.9:c.15440A>G MANE Select ENSP00000384582.2:p.Asp5147Gly
NM_032119.3:c.15440A>G NP_115495.3:p.Asp5147Gly
NR_003149.1:n.15453A>G
NR_003149.2:n.15456A>G
ENST00000405460.6:c.15440A>G ENSP00000384582.2:p.Asp5147Gly
ENST00000425867.2:c.2423A>G ENSP00000392618.2:p.Asp808Gly
ENST00000425867.3:c.4394A>G ENSP00000392618.3:p.Asp1465Gly
ENST00000638510.1:n.2707A>G
ENST00000639431.1:c.265+134491A>G ENSP00000491057.1:n.265+134491A>G
ENST00000640407.1:c.1850A>G ENSP00000491425.1:p.Asp617Gly
XM_011543675.1:c.15437A>G XP_011541977.1:p.Asp5146Gly
XM_011543676.1:c.15359A>G XP_011541978.1:p.Asp5120Gly
XM_011543677.1:c.12743A>G XP_011541979.1:p.Asp4248Gly
XM_017009963.2:c.15461A>G XP_016865452.1:p.Asp5154Gly
XM_017009964.2:c.15458A>G XP_016865453.1:p.Asp5153Gly
XM_017009965.1:c.15458A>G XP_016865454.1:p.Asp5153Gly
XM_017009966.2:c.15380A>G XP_016865455.1:p.Asp5127Gly
XM_017009967.1:c.15365A>G XP_016865456.1:p.Asp5122Gly
XM_017009968.2:c.15281A>G XP_016865457.1:p.Asp5094Gly
XM_017009969.2:c.15461A>G XP_016865458.1:p.Asp5154Gly
XM_017009971.2:c.*394A>G XP_016865460.1:n.*394A>G
XM_017009972.1:c.8579A>G XP_016865461.1:p.Asp2860Gly
XM_017009973.1:c.8558A>G XP_016865462.1:p.Asp2853Gly